Atlas of X-linked intellectual disability syndromes /:
The Atlas of X-Linked Intellectual Disability Syndromes is a comprehensive and up-to-date summary of the clinically distinctive disorders caused by genes on the X chromosome. Clinical and laboratory data on 150 syndromes are presented in a concise and consistent manner. Each syndrome is defined and...
Gespeichert in:
| 1. Verfasser: | |
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| Weitere Verfasser: | , |
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Oxford ; New York :
Oxford University Press,
[2012]
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| Ausgabe: | Second edition. |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Zusammenfassung: | The Atlas of X-Linked Intellectual Disability Syndromes is a comprehensive and up-to-date summary of the clinically distinctive disorders caused by genes on the X chromosome. Clinical and laboratory data on 150 syndromes are presented in a concise and consistent manner. Each syndrome is defined and information is provided on somatic features, growth and development, neurological signs, cognitive performance, imaging and other laboratory findings, and when possible, the nature and localization of the responsible gene. Craniofacial and other somatic findings are extensively illustrated. A differ. |
| Beschreibung: | 1 online resource (xvii, 344 pages) : illustrations |
| Bibliographie: | Includes bibliographical references and index. |
| ISBN: | 9780199811861 0199811865 |
Internformat
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| 100 | 1 | |a Stevenson, Roger E., |d 1940- |1 https://id.oclc.org/worldcat/entity/E39PCjHFdmyqJtVRDrh6hQRK7d |0 http://id.loc.gov/authorities/names/n92805492 | |
| 245 | 1 | 0 | |a Atlas of X-linked intellectual disability syndromes / |c Roger E. Stevenson, Charles E. Schwartz, and R. Curtis Rogers. |
| 250 | |a Second edition. | ||
| 264 | 1 | |a Oxford ; |a New York : |b Oxford University Press, |c [2012] | |
| 264 | 4 | |c ©2012 | |
| 300 | |a 1 online resource (xvii, 344 pages) : |b illustrations | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 504 | |a Includes bibliographical references and index. | ||
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |a Cover; TABLE OF CONTENTS; FOREWORD; PREFACE; AARSKOG SYNDROME; ABIDI SYNDROME; ADRENOLEUKODYSTROPHY; AGENESIS OF THE CORPUS CALLOSUM, X-LINKED; AHMAD SYNDROME; AICARDI SYNDROME; ALLAN-HERNDON-DUDLEY SYNDROME; ALPHA-THALASSEMIA INTELLECTUAL DISABILITY (SEE ALSO ATRX-ASSOCIATED XLID); AP1S2-ASSOCIATED XLID; APAK ATAXIA-SPASTIC DIPLEGIA SYNDROME; ARMFIELD SYNDROME; ARTS SYNDROME; ARX-ASSOCIATED XLID; ATAXIA-DEAFNESS-DEMENTIA, X-LINKED; ATKIN-FLAITZ SYNDROME; ATRX-ASSOCIATED XLID; BERGIA CARDIOMYOPATHY; BERTINI SYNDROME; BÖRJESON-FORSSMAN-LEHMANN SYNDROME; BRANCHIAL ARCH SYNDROME, X-LINKED. | |
| 505 | 8 | |a Cantu syndromecarpenter-waziri syndrome (see also atrx-associated xlid); cerebro-cerebello-coloboma syndrome; cerebro-oculo-genital syndrome; cerebro-palato-cardiac syndrome (see also renpenning syndrome); charcot-marie-tooth neuropathy, cowchock variant; charcot-marie-tooth neuropathy, ionasescu variant; chassaing-lacombe chondrodysplasia; christian syndrome; christianson syndrome; chudley-lowry syndrome (see also atrx-associated xlid); ck syndrome; clark-baraitser syndrome; coffin-lowry syndrome; cornelia de lange syndrome, x-linked; craniofacioskeletal syndrome. | |
| 505 | 8 | |a Creatine transporter deficiencyduchenne muscular dystrophy; dyskeratosis congenita; epilepsy-intellectual disability in females (eidf); fitzsimmons syndrome; flna-associated xlid; fragile x syndrome; giuffrè-tsukahara syndrome; glycerol kinase deficiency; golabi-ito-hall syndrome: (see also renpenning syndrome); goldblatt spastic paraplegia syndrome; goltz syndrome; graham anophthalmia syndrome; gustavson syndrome; hall orofacial syndrome; hereditary bullous dystrophy, x-linked; holmes-gang syndrome (see also atrx-associated xlid); homfray seizures-contractures; hyde-forster syndrome. | |
| 505 | 8 | |a Hydranencephaly with abnormal genitalia (see also arx-associated xlid)hydrocephaly-cerebellar agenesis syndrome; hydrocephaly-masa spectrum; hypoparathyroidism, x-linked; incontinentia pigmenti; juberg-marsidi-brooks syndrome; kang syndrome; lenz microphthalmia syndrome; lesch-nyhan syndrome; lissencephaly and abnormal genitalia, x-linked (see also arx-associated xlid); lissencephaly, x-linked; lowe syndrome; lujan syndrome; martin-probst syndrome; mehmo syndrome; menkes syndrome; midas syndrome; miles-carpenter syndrome; mohr-tranebjaerg syndrome; monoamine oxidase-a deficiency. | |
| 505 | 8 | |a Mucopolysaccharidosis iiamyotubular myopathy; n-alpha-acetyltransferase deficiency; nance-horan syndrome; norrie disease; opitz fg syndrome; optic atrophy, x-linked; oral-facial-digital syndrome i; ornithine transcarbamoylase deficiency; otopalatodigital syndrome i (see also flna-associated xlid); otopalatodigital syndrome ii (see also flna-associated xlid); paine syndrome; pallister w syndrome; partington syndrome (see also arx-associated xlid); pelizaeus-merzbacher syndrome; periventricular nodular heterotopia (see also flna-associated xlid); pettigrew syndrome. | |
| 520 | |a The Atlas of X-Linked Intellectual Disability Syndromes is a comprehensive and up-to-date summary of the clinically distinctive disorders caused by genes on the X chromosome. Clinical and laboratory data on 150 syndromes are presented in a concise and consistent manner. Each syndrome is defined and information is provided on somatic features, growth and development, neurological signs, cognitive performance, imaging and other laboratory findings, and when possible, the nature and localization of the responsible gene. Craniofacial and other somatic findings are extensively illustrated. A differ. | ||
| 650 | 0 | |a X-linked mental retardation |v Atlases. | |
| 650 | 0 | |a X-linked mental retardation. |0 http://id.loc.gov/authorities/subjects/sh99002289 | |
| 650 | 1 | 2 | |a Mental Retardation, X-Linked |
| 650 | 6 | |a Déficience intellectuelle liée au chromosome X |v Atlas. | |
| 650 | 6 | |a Déficience intellectuelle liée au chromosome X. | |
| 650 | 7 | |a HEALTH & FITNESS |x Diseases |x General. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Clinical Medicine. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Diseases. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Evidence-Based Medicine. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Internal Medicine. |2 bisacsh | |
| 650 | 7 | |a X-linked mental retardation |2 fast | |
| 655 | 2 | |a Atlas | |
| 655 | 7 | |a atlases. |2 aat | |
| 655 | 7 | |a Scientific atlases |2 fast | |
| 655 | 7 | |a Atlases |2 fast | |
| 655 | 7 | |a Atlases. |2 lcgft |0 http://id.loc.gov/authorities/genreForms/gf2011026058 | |
| 655 | 7 | |a Atlas. |2 rvmgf | |
| 700 | 1 | |a Schwartz, Charles E. | |
| 700 | 1 | |a Rogers, R. Curtis |q (Richard Curtis), |d 1953- |1 https://id.oclc.org/worldcat/entity/E39PCjMqbWbDGphbTTpjcQWjyd |0 http://id.loc.gov/authorities/names/n2011182290 | |
| 700 | 1 | |a Stevenson, Roger E., |d 1940- |t X-linked mental retardation. | |
| 758 | |i has work: |a Atlas of X-linked intellectual disability syndromes (Text) |1 https://id.oclc.org/worldcat/entity/E39PCGwYJJHhRC46mtBcffm9cK |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
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| author | Stevenson, Roger E., 1940- |
| author2 | Schwartz, Charles E. Rogers, R. Curtis (Richard Curtis), 1953- Stevenson, Roger E., 1940- |
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| author_GND | http://id.loc.gov/authorities/names/n92805492 http://id.loc.gov/authorities/names/n2011182290 |
| author_facet | Stevenson, Roger E., 1940- Schwartz, Charles E. Rogers, R. Curtis (Richard Curtis), 1953- Stevenson, Roger E., 1940- |
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| author_sort | Stevenson, Roger E., 1940- |
| author_variant | r e s re res |
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| bvnumber | localFWS |
| callnumber-first | R - Medicine |
| callnumber-label | RC574 |
| callnumber-raw | RC574 .S77 2012eb |
| callnumber-search | RC574 .S77 2012eb |
| callnumber-sort | RC 3574 S77 42012EB |
| callnumber-subject | RC - Internal Medicine |
| collection | ZDB-4-EBA |
| contents | Cover; TABLE OF CONTENTS; FOREWORD; PREFACE; AARSKOG SYNDROME; ABIDI SYNDROME; ADRENOLEUKODYSTROPHY; AGENESIS OF THE CORPUS CALLOSUM, X-LINKED; AHMAD SYNDROME; AICARDI SYNDROME; ALLAN-HERNDON-DUDLEY SYNDROME; ALPHA-THALASSEMIA INTELLECTUAL DISABILITY (SEE ALSO ATRX-ASSOCIATED XLID); AP1S2-ASSOCIATED XLID; APAK ATAXIA-SPASTIC DIPLEGIA SYNDROME; ARMFIELD SYNDROME; ARTS SYNDROME; ARX-ASSOCIATED XLID; ATAXIA-DEAFNESS-DEMENTIA, X-LINKED; ATKIN-FLAITZ SYNDROME; ATRX-ASSOCIATED XLID; BERGIA CARDIOMYOPATHY; BERTINI SYNDROME; BÖRJESON-FORSSMAN-LEHMANN SYNDROME; BRANCHIAL ARCH SYNDROME, X-LINKED. Cantu syndromecarpenter-waziri syndrome (see also atrx-associated xlid); cerebro-cerebello-coloboma syndrome; cerebro-oculo-genital syndrome; cerebro-palato-cardiac syndrome (see also renpenning syndrome); charcot-marie-tooth neuropathy, cowchock variant; charcot-marie-tooth neuropathy, ionasescu variant; chassaing-lacombe chondrodysplasia; christian syndrome; christianson syndrome; chudley-lowry syndrome (see also atrx-associated xlid); ck syndrome; clark-baraitser syndrome; coffin-lowry syndrome; cornelia de lange syndrome, x-linked; craniofacioskeletal syndrome. Creatine transporter deficiencyduchenne muscular dystrophy; dyskeratosis congenita; epilepsy-intellectual disability in females (eidf); fitzsimmons syndrome; flna-associated xlid; fragile x syndrome; giuffrè-tsukahara syndrome; glycerol kinase deficiency; golabi-ito-hall syndrome: (see also renpenning syndrome); goldblatt spastic paraplegia syndrome; goltz syndrome; graham anophthalmia syndrome; gustavson syndrome; hall orofacial syndrome; hereditary bullous dystrophy, x-linked; holmes-gang syndrome (see also atrx-associated xlid); homfray seizures-contractures; hyde-forster syndrome. Hydranencephaly with abnormal genitalia (see also arx-associated xlid)hydrocephaly-cerebellar agenesis syndrome; hydrocephaly-masa spectrum; hypoparathyroidism, x-linked; incontinentia pigmenti; juberg-marsidi-brooks syndrome; kang syndrome; lenz microphthalmia syndrome; lesch-nyhan syndrome; lissencephaly and abnormal genitalia, x-linked (see also arx-associated xlid); lissencephaly, x-linked; lowe syndrome; lujan syndrome; martin-probst syndrome; mehmo syndrome; menkes syndrome; midas syndrome; miles-carpenter syndrome; mohr-tranebjaerg syndrome; monoamine oxidase-a deficiency. Mucopolysaccharidosis iiamyotubular myopathy; n-alpha-acetyltransferase deficiency; nance-horan syndrome; norrie disease; opitz fg syndrome; optic atrophy, x-linked; oral-facial-digital syndrome i; ornithine transcarbamoylase deficiency; otopalatodigital syndrome i (see also flna-associated xlid); otopalatodigital syndrome ii (see also flna-associated xlid); paine syndrome; pallister w syndrome; partington syndrome (see also arx-associated xlid); pelizaeus-merzbacher syndrome; periventricular nodular heterotopia (see also flna-associated xlid); pettigrew syndrome. |
| ctrlnum | (OCoLC)859536495 |
| dewey-full | 616.85/88042 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 616 - Diseases |
| dewey-raw | 616.85/88042 |
| dewey-search | 616.85/88042 |
| dewey-sort | 3616.85 588042 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| edition | Second edition. |
| format | Electronic eBook |
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| genre | Atlas atlases. aat Scientific atlases fast Atlases fast Atlases. lcgft http://id.loc.gov/authorities/genreForms/gf2011026058 Atlas. rvmgf |
| genre_facet | Atlas atlases. Scientific atlases Atlases Atlases. Atlas. |
| id | ZDB-4-EBA-ocn859536495 |
| illustrated | Illustrated |
| indexdate | 2024-11-27T13:25:33Z |
| institution | BVB |
| isbn | 9780199811861 0199811865 |
| language | English |
| oclc_num | 859536495 |
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| owner_facet | MAIN DE-863 DE-BY-FWS |
| physical | 1 online resource (xvii, 344 pages) : illustrations |
| psigel | ZDB-4-EBA |
| publishDate | 2012 |
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| publisher | Oxford University Press, |
| record_format | marc |
| spelling | Stevenson, Roger E., 1940- https://id.oclc.org/worldcat/entity/E39PCjHFdmyqJtVRDrh6hQRK7d http://id.loc.gov/authorities/names/n92805492 Atlas of X-linked intellectual disability syndromes / Roger E. Stevenson, Charles E. Schwartz, and R. Curtis Rogers. Second edition. Oxford ; New York : Oxford University Press, [2012] ©2012 1 online resource (xvii, 344 pages) : illustrations text txt rdacontent computer c rdamedia online resource cr rdacarrier Includes bibliographical references and index. Print version record. Cover; TABLE OF CONTENTS; FOREWORD; PREFACE; AARSKOG SYNDROME; ABIDI SYNDROME; ADRENOLEUKODYSTROPHY; AGENESIS OF THE CORPUS CALLOSUM, X-LINKED; AHMAD SYNDROME; AICARDI SYNDROME; ALLAN-HERNDON-DUDLEY SYNDROME; ALPHA-THALASSEMIA INTELLECTUAL DISABILITY (SEE ALSO ATRX-ASSOCIATED XLID); AP1S2-ASSOCIATED XLID; APAK ATAXIA-SPASTIC DIPLEGIA SYNDROME; ARMFIELD SYNDROME; ARTS SYNDROME; ARX-ASSOCIATED XLID; ATAXIA-DEAFNESS-DEMENTIA, X-LINKED; ATKIN-FLAITZ SYNDROME; ATRX-ASSOCIATED XLID; BERGIA CARDIOMYOPATHY; BERTINI SYNDROME; BÖRJESON-FORSSMAN-LEHMANN SYNDROME; BRANCHIAL ARCH SYNDROME, X-LINKED. Cantu syndromecarpenter-waziri syndrome (see also atrx-associated xlid); cerebro-cerebello-coloboma syndrome; cerebro-oculo-genital syndrome; cerebro-palato-cardiac syndrome (see also renpenning syndrome); charcot-marie-tooth neuropathy, cowchock variant; charcot-marie-tooth neuropathy, ionasescu variant; chassaing-lacombe chondrodysplasia; christian syndrome; christianson syndrome; chudley-lowry syndrome (see also atrx-associated xlid); ck syndrome; clark-baraitser syndrome; coffin-lowry syndrome; cornelia de lange syndrome, x-linked; craniofacioskeletal syndrome. Creatine transporter deficiencyduchenne muscular dystrophy; dyskeratosis congenita; epilepsy-intellectual disability in females (eidf); fitzsimmons syndrome; flna-associated xlid; fragile x syndrome; giuffrè-tsukahara syndrome; glycerol kinase deficiency; golabi-ito-hall syndrome: (see also renpenning syndrome); goldblatt spastic paraplegia syndrome; goltz syndrome; graham anophthalmia syndrome; gustavson syndrome; hall orofacial syndrome; hereditary bullous dystrophy, x-linked; holmes-gang syndrome (see also atrx-associated xlid); homfray seizures-contractures; hyde-forster syndrome. Hydranencephaly with abnormal genitalia (see also arx-associated xlid)hydrocephaly-cerebellar agenesis syndrome; hydrocephaly-masa spectrum; hypoparathyroidism, x-linked; incontinentia pigmenti; juberg-marsidi-brooks syndrome; kang syndrome; lenz microphthalmia syndrome; lesch-nyhan syndrome; lissencephaly and abnormal genitalia, x-linked (see also arx-associated xlid); lissencephaly, x-linked; lowe syndrome; lujan syndrome; martin-probst syndrome; mehmo syndrome; menkes syndrome; midas syndrome; miles-carpenter syndrome; mohr-tranebjaerg syndrome; monoamine oxidase-a deficiency. Mucopolysaccharidosis iiamyotubular myopathy; n-alpha-acetyltransferase deficiency; nance-horan syndrome; norrie disease; opitz fg syndrome; optic atrophy, x-linked; oral-facial-digital syndrome i; ornithine transcarbamoylase deficiency; otopalatodigital syndrome i (see also flna-associated xlid); otopalatodigital syndrome ii (see also flna-associated xlid); paine syndrome; pallister w syndrome; partington syndrome (see also arx-associated xlid); pelizaeus-merzbacher syndrome; periventricular nodular heterotopia (see also flna-associated xlid); pettigrew syndrome. The Atlas of X-Linked Intellectual Disability Syndromes is a comprehensive and up-to-date summary of the clinically distinctive disorders caused by genes on the X chromosome. Clinical and laboratory data on 150 syndromes are presented in a concise and consistent manner. Each syndrome is defined and information is provided on somatic features, growth and development, neurological signs, cognitive performance, imaging and other laboratory findings, and when possible, the nature and localization of the responsible gene. Craniofacial and other somatic findings are extensively illustrated. A differ. X-linked mental retardation Atlases. X-linked mental retardation. http://id.loc.gov/authorities/subjects/sh99002289 Mental Retardation, X-Linked Déficience intellectuelle liée au chromosome X Atlas. Déficience intellectuelle liée au chromosome X. HEALTH & FITNESS Diseases General. bisacsh MEDICAL Clinical Medicine. bisacsh MEDICAL Diseases. bisacsh MEDICAL Evidence-Based Medicine. bisacsh MEDICAL Internal Medicine. bisacsh X-linked mental retardation fast Atlas atlases. aat Scientific atlases fast Atlases fast Atlases. lcgft http://id.loc.gov/authorities/genreForms/gf2011026058 Atlas. rvmgf Schwartz, Charles E. Rogers, R. Curtis (Richard Curtis), 1953- https://id.oclc.org/worldcat/entity/E39PCjMqbWbDGphbTTpjcQWjyd http://id.loc.gov/authorities/names/n2011182290 Stevenson, Roger E., 1940- X-linked mental retardation. has work: Atlas of X-linked intellectual disability syndromes (Text) https://id.oclc.org/worldcat/entity/E39PCGwYJJHhRC46mtBcffm9cK https://id.oclc.org/worldcat/ontology/hasWork Print version: Stevenson, Roger E., 1940- Atlas of X-linked intellectual disability syndromes. Second edition 9780199811793 (DLC) 2011024318 (OCoLC)731127483 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=646810 Volltext |
| spellingShingle | Stevenson, Roger E., 1940- Atlas of X-linked intellectual disability syndromes / Cover; TABLE OF CONTENTS; FOREWORD; PREFACE; AARSKOG SYNDROME; ABIDI SYNDROME; ADRENOLEUKODYSTROPHY; AGENESIS OF THE CORPUS CALLOSUM, X-LINKED; AHMAD SYNDROME; AICARDI SYNDROME; ALLAN-HERNDON-DUDLEY SYNDROME; ALPHA-THALASSEMIA INTELLECTUAL DISABILITY (SEE ALSO ATRX-ASSOCIATED XLID); AP1S2-ASSOCIATED XLID; APAK ATAXIA-SPASTIC DIPLEGIA SYNDROME; ARMFIELD SYNDROME; ARTS SYNDROME; ARX-ASSOCIATED XLID; ATAXIA-DEAFNESS-DEMENTIA, X-LINKED; ATKIN-FLAITZ SYNDROME; ATRX-ASSOCIATED XLID; BERGIA CARDIOMYOPATHY; BERTINI SYNDROME; BÖRJESON-FORSSMAN-LEHMANN SYNDROME; BRANCHIAL ARCH SYNDROME, X-LINKED. Cantu syndromecarpenter-waziri syndrome (see also atrx-associated xlid); cerebro-cerebello-coloboma syndrome; cerebro-oculo-genital syndrome; cerebro-palato-cardiac syndrome (see also renpenning syndrome); charcot-marie-tooth neuropathy, cowchock variant; charcot-marie-tooth neuropathy, ionasescu variant; chassaing-lacombe chondrodysplasia; christian syndrome; christianson syndrome; chudley-lowry syndrome (see also atrx-associated xlid); ck syndrome; clark-baraitser syndrome; coffin-lowry syndrome; cornelia de lange syndrome, x-linked; craniofacioskeletal syndrome. Creatine transporter deficiencyduchenne muscular dystrophy; dyskeratosis congenita; epilepsy-intellectual disability in females (eidf); fitzsimmons syndrome; flna-associated xlid; fragile x syndrome; giuffrè-tsukahara syndrome; glycerol kinase deficiency; golabi-ito-hall syndrome: (see also renpenning syndrome); goldblatt spastic paraplegia syndrome; goltz syndrome; graham anophthalmia syndrome; gustavson syndrome; hall orofacial syndrome; hereditary bullous dystrophy, x-linked; holmes-gang syndrome (see also atrx-associated xlid); homfray seizures-contractures; hyde-forster syndrome. Hydranencephaly with abnormal genitalia (see also arx-associated xlid)hydrocephaly-cerebellar agenesis syndrome; hydrocephaly-masa spectrum; hypoparathyroidism, x-linked; incontinentia pigmenti; juberg-marsidi-brooks syndrome; kang syndrome; lenz microphthalmia syndrome; lesch-nyhan syndrome; lissencephaly and abnormal genitalia, x-linked (see also arx-associated xlid); lissencephaly, x-linked; lowe syndrome; lujan syndrome; martin-probst syndrome; mehmo syndrome; menkes syndrome; midas syndrome; miles-carpenter syndrome; mohr-tranebjaerg syndrome; monoamine oxidase-a deficiency. Mucopolysaccharidosis iiamyotubular myopathy; n-alpha-acetyltransferase deficiency; nance-horan syndrome; norrie disease; opitz fg syndrome; optic atrophy, x-linked; oral-facial-digital syndrome i; ornithine transcarbamoylase deficiency; otopalatodigital syndrome i (see also flna-associated xlid); otopalatodigital syndrome ii (see also flna-associated xlid); paine syndrome; pallister w syndrome; partington syndrome (see also arx-associated xlid); pelizaeus-merzbacher syndrome; periventricular nodular heterotopia (see also flna-associated xlid); pettigrew syndrome. X-linked mental retardation Atlases. X-linked mental retardation. http://id.loc.gov/authorities/subjects/sh99002289 Mental Retardation, X-Linked Déficience intellectuelle liée au chromosome X Atlas. Déficience intellectuelle liée au chromosome X. HEALTH & FITNESS Diseases General. bisacsh MEDICAL Clinical Medicine. bisacsh MEDICAL Diseases. bisacsh MEDICAL Evidence-Based Medicine. bisacsh MEDICAL Internal Medicine. bisacsh X-linked mental retardation fast |
| subject_GND | http://id.loc.gov/authorities/subjects/sh99002289 http://id.loc.gov/authorities/genreForms/gf2011026058 |
| title | Atlas of X-linked intellectual disability syndromes / |
| title_alt | X-linked mental retardation. |
| title_auth | Atlas of X-linked intellectual disability syndromes / |
| title_exact_search | Atlas of X-linked intellectual disability syndromes / |
| title_full | Atlas of X-linked intellectual disability syndromes / Roger E. Stevenson, Charles E. Schwartz, and R. Curtis Rogers. |
| title_fullStr | Atlas of X-linked intellectual disability syndromes / Roger E. Stevenson, Charles E. Schwartz, and R. Curtis Rogers. |
| title_full_unstemmed | Atlas of X-linked intellectual disability syndromes / Roger E. Stevenson, Charles E. Schwartz, and R. Curtis Rogers. |
| title_short | Atlas of X-linked intellectual disability syndromes / |
| title_sort | atlas of x linked intellectual disability syndromes |
| topic | X-linked mental retardation Atlases. X-linked mental retardation. http://id.loc.gov/authorities/subjects/sh99002289 Mental Retardation, X-Linked Déficience intellectuelle liée au chromosome X Atlas. Déficience intellectuelle liée au chromosome X. HEALTH & FITNESS Diseases General. bisacsh MEDICAL Clinical Medicine. bisacsh MEDICAL Diseases. bisacsh MEDICAL Evidence-Based Medicine. bisacsh MEDICAL Internal Medicine. bisacsh X-linked mental retardation fast |
| topic_facet | X-linked mental retardation Atlases. X-linked mental retardation. Mental Retardation, X-Linked Déficience intellectuelle liée au chromosome X Atlas. Déficience intellectuelle liée au chromosome X. HEALTH & FITNESS Diseases General. MEDICAL Clinical Medicine. MEDICAL Diseases. MEDICAL Evidence-Based Medicine. MEDICAL Internal Medicine. X-linked mental retardation Atlas atlases. Scientific atlases Atlases Atlases. Atlas. |
| url | https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=646810 |
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