The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis:
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , , , , , , , , , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Erlangen
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
2011
|
| Online-Zugang: | Volltext Volltext Volltext |
| Beschreibung: | Aus: Journal of Medical Genetics 48.6 (2011): S. 396-406. <http://jmg.bmj.com/content/48/6/396> Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence or a national licence (funded by the DFG, German Research Foundation) respectively. |
| Beschreibung: | 1 Online-Ressource |
| Format: | Langzeitarchivierung gewährleistet, LZA |
Internformat
MARC
| LEADER | 00000nmm a2200000zc 4500 | ||
|---|---|---|---|
| 001 | BV043897471 | ||
| 003 | DE-604 | ||
| 005 | 00000000000000.0 | ||
| 007 | cr|uuu---uuuuu | ||
| 008 | 161124s2011 gw |||| o||u| ||||||eng d | ||
| 015 | |a 16,O12 |2 dnb | ||
| 016 | 7 | |a 1119450276 |2 DE-101 | |
| 024 | 7 | |a urn:nbn:de:bvb:29-opus4-77870 |2 urn | |
| 035 | |a (OCoLC)965687356 | ||
| 035 | |a (DE-599)DNB1119450276 | ||
| 040 | |a DE-604 |b ger |e rda | ||
| 041 | 0 | |a eng | |
| 044 | |a gw |c XA-DE-BY | ||
| 049 | |a DE-29 | ||
| 082 | 0 | |a 610 |2 23 | |
| 084 | |a 610 |2 sdnb | ||
| 100 | 1 | |a Kortüm, Fanny |e Verfasser |4 aut | |
| 245 | 1 | 0 | |a The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis |c Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B. Dobyns |
| 264 | 1 | |a Erlangen |b Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) |c 2011 | |
| 300 | |a 1 Online-Ressource | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b c |2 rdamedia | ||
| 338 | |b cr |2 rdacarrier | ||
| 500 | |a Aus: Journal of Medical Genetics 48.6 (2011): S. 396-406. <http://jmg.bmj.com/content/48/6/396> | ||
| 500 | |a Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. | ||
| 500 | |a This publication is with permission of the rights owner freely accessible due to an Alliance licence or a national licence (funded by the DFG, German Research Foundation) respectively. | ||
| 538 | |a Langzeitarchivierung gewährleistet, LZA | ||
| 700 | 1 | |a Das, Soma |e Verfasser |4 aut | |
| 700 | 1 | |a Flindt, Max |e Verfasser |4 aut | |
| 700 | 1 | |a Morris-Rosendahl, Deborah J. |e Verfasser |4 aut | |
| 700 | 1 | |a Stefanova, Irina |e Verfasser |4 aut | |
| 700 | 1 | |a Goldstein, Amy |e Verfasser |4 aut | |
| 700 | 1 | |a Horn, Denise |e Verfasser |4 aut | |
| 700 | 1 | |a Klopocki, Eva |e Verfasser |4 aut | |
| 700 | 1 | |a Kluger, Gerhard |e Verfasser |4 aut | |
| 700 | 1 | |a Martin, Peter |e Verfasser |4 aut | |
| 700 | 1 | |a Rauch, Anita |e Verfasser |4 aut | |
| 700 | 1 | |a Roumer, Agathe |e Verfasser |4 aut | |
| 700 | 1 | |a Saitta, Sulagna |e Verfasser |4 aut | |
| 700 | 1 | |a Walsh, Laurence E. |e Verfasser |4 aut | |
| 700 | 1 | |a Wieczorek, Dagmar |e Verfasser |4 aut | |
| 700 | 1 | |a Uyanik, Gökhan |e Verfasser |4 aut | |
| 700 | 1 | |a Kutsche, Kerstin |e Verfasser |4 aut | |
| 700 | 1 | |a Dobyns, William B. |e Verfasser |4 aut | |
| 856 | 4 | 0 | |u https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-77870 |x Resolving-System |z kostenfrei |3 Volltext |
| 856 | 4 | 0 | |u http://d-nb.info/1119450276/34 |x Langzeitarchivierung Nationalbibliothek |z kostenfrei |3 Volltext |
| 856 | 4 | 0 | |u https://open.fau.de/handle/openfau/7787 |x Verlag |z kostenfrei |3 Volltext |
| 912 | |a ebook | ||
| 999 | |a oai:aleph.bib-bvb.de:BVB01-029306808 | ||
Datensatz im Suchindex
| _version_ | 1804176798912610304 |
|---|---|
| any_adam_object | |
| author | Kortüm, Fanny Das, Soma Flindt, Max Morris-Rosendahl, Deborah J. Stefanova, Irina Goldstein, Amy Horn, Denise Klopocki, Eva Kluger, Gerhard Martin, Peter Rauch, Anita Roumer, Agathe Saitta, Sulagna Walsh, Laurence E. Wieczorek, Dagmar Uyanik, Gökhan Kutsche, Kerstin Dobyns, William B. |
| author_facet | Kortüm, Fanny Das, Soma Flindt, Max Morris-Rosendahl, Deborah J. Stefanova, Irina Goldstein, Amy Horn, Denise Klopocki, Eva Kluger, Gerhard Martin, Peter Rauch, Anita Roumer, Agathe Saitta, Sulagna Walsh, Laurence E. Wieczorek, Dagmar Uyanik, Gökhan Kutsche, Kerstin Dobyns, William B. |
| author_role | aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut |
| author_sort | Kortüm, Fanny |
| author_variant | f k fk s d sd m f mf d j m r djm djmr i s is a g ag d h dh e k ek g k gk p m pm a r ar a r ar s s ss l e w le lew d w dw g u gu k k kk w b d wb wbd |
| building | Verbundindex |
| bvnumber | BV043897471 |
| collection | ebook |
| ctrlnum | (OCoLC)965687356 (DE-599)DNB1119450276 |
| dewey-full | 610 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 610 - Medicine and health |
| dewey-raw | 610 |
| dewey-search | 610 |
| dewey-sort | 3610 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| format | Electronic eBook |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02966nmm a2200613zc 4500</leader><controlfield tag="001">BV043897471</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">161124s2011 gw |||| o||u| ||||||eng d</controlfield><datafield tag="015" ind1=" " ind2=" "><subfield code="a">16,O12</subfield><subfield code="2">dnb</subfield></datafield><datafield tag="016" ind1="7" ind2=" "><subfield code="a">1119450276</subfield><subfield code="2">DE-101</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">urn:nbn:de:bvb:29-opus4-77870</subfield><subfield code="2">urn</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)965687356</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DNB1119450276</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">gw</subfield><subfield code="c">XA-DE-BY</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-29</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">610</subfield><subfield code="2">23</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">610</subfield><subfield code="2">sdnb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Kortüm, Fanny</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis</subfield><subfield code="c">Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B. Dobyns</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Erlangen</subfield><subfield code="b">Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)</subfield><subfield code="c">2011</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Aus: Journal of Medical Genetics 48.6 (2011): S. 396-406. <http://jmg.bmj.com/content/48/6/396></subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">This publication is with permission of the rights owner freely accessible due to an Alliance licence or a national licence (funded by the DFG, German Research Foundation) respectively.</subfield></datafield><datafield tag="538" ind1=" " ind2=" "><subfield code="a">Langzeitarchivierung gewährleistet, LZA</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Das, Soma</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Flindt, Max</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Morris-Rosendahl, Deborah J.</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Stefanova, Irina</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Goldstein, Amy</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Horn, Denise</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Klopocki, Eva</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kluger, Gerhard</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Martin, Peter</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Rauch, Anita</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Roumer, Agathe</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Saitta, Sulagna</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Walsh, Laurence E.</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Wieczorek, Dagmar</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Uyanik, Gökhan</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kutsche, Kerstin</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Dobyns, William B.</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-77870</subfield><subfield code="x">Resolving-System</subfield><subfield code="z">kostenfrei</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://d-nb.info/1119450276/34</subfield><subfield code="x">Langzeitarchivierung Nationalbibliothek</subfield><subfield code="z">kostenfrei</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://open.fau.de/handle/openfau/7787</subfield><subfield code="x">Verlag</subfield><subfield code="z">kostenfrei</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ebook</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-029306808</subfield></datafield></record></collection> |
| id | DE-604.BV043897471 |
| illustrated | Not Illustrated |
| indexdate | 2024-07-10T07:37:55Z |
| institution | BVB |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-029306808 |
| oclc_num | 965687356 |
| open_access_boolean | 1 |
| owner | DE-29 |
| owner_facet | DE-29 |
| physical | 1 Online-Ressource |
| psigel | ebook |
| publishDate | 2011 |
| publishDateSearch | 2011 |
| publishDateSort | 2011 |
| publisher | Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) |
| record_format | marc |
| spelling | Kortüm, Fanny Verfasser aut The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B. Dobyns Erlangen Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) 2011 1 Online-Ressource txt rdacontent c rdamedia cr rdacarrier Aus: Journal of Medical Genetics 48.6 (2011): S. 396-406. <http://jmg.bmj.com/content/48/6/396> Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence or a national licence (funded by the DFG, German Research Foundation) respectively. Langzeitarchivierung gewährleistet, LZA Das, Soma Verfasser aut Flindt, Max Verfasser aut Morris-Rosendahl, Deborah J. Verfasser aut Stefanova, Irina Verfasser aut Goldstein, Amy Verfasser aut Horn, Denise Verfasser aut Klopocki, Eva Verfasser aut Kluger, Gerhard Verfasser aut Martin, Peter Verfasser aut Rauch, Anita Verfasser aut Roumer, Agathe Verfasser aut Saitta, Sulagna Verfasser aut Walsh, Laurence E. Verfasser aut Wieczorek, Dagmar Verfasser aut Uyanik, Gökhan Verfasser aut Kutsche, Kerstin Verfasser aut Dobyns, William B. Verfasser aut https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-77870 Resolving-System kostenfrei Volltext http://d-nb.info/1119450276/34 Langzeitarchivierung Nationalbibliothek kostenfrei Volltext https://open.fau.de/handle/openfau/7787 Verlag kostenfrei Volltext |
| spellingShingle | Kortüm, Fanny Das, Soma Flindt, Max Morris-Rosendahl, Deborah J. Stefanova, Irina Goldstein, Amy Horn, Denise Klopocki, Eva Kluger, Gerhard Martin, Peter Rauch, Anita Roumer, Agathe Saitta, Sulagna Walsh, Laurence E. Wieczorek, Dagmar Uyanik, Gökhan Kutsche, Kerstin Dobyns, William B. The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis |
| title | The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis |
| title_auth | The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis |
| title_exact_search | The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis |
| title_full | The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B. Dobyns |
| title_fullStr | The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B. Dobyns |
| title_full_unstemmed | The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B. Dobyns |
| title_short | The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis |
| title_sort | the core foxg1 syndrome phenotype consists of postnatal microcephaly severe mental retardation absent language dyskinesia and corpus callosum hypogenesis |
| url | https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-77870 http://d-nb.info/1119450276/34 https://open.fau.de/handle/openfau/7787 |
| work_keys_str_mv | AT kortumfanny thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT dassoma thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT flindtmax thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT morrisrosendahldeborahj thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT stefanovairina thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT goldsteinamy thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT horndenise thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT klopockieva thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT klugergerhard thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT martinpeter thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT rauchanita thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT roumeragathe thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT saittasulagna thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT walshlaurencee thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT wieczorekdagmar thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT uyanikgokhan thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT kutschekerstin thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis AT dobynswilliamb thecorefoxg1syndromephenotypeconsistsofpostnatalmicrocephalyseverementalretardationabsentlanguagedyskinesiaandcorpuscallosumhypogenesis |