A song of rest: arranged as a trio, with pianoforte accompaniment
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Elektronisch Partitur Buch |
| Sprache: | English |
| Veröffentlicht: |
[London, England]
Novello & Company
[1955]
|
| Schriftenreihe: | Novello's octavo edition of trios, &c., for female voices
trios 521 |
| Schlagworte: | |
| Online-Zugang: | BSB01 URL des Erstveröffentlichers Inhaltsverzeichnis |
| Beschreibung: | Title from title page (viewed March 27, 2019) Written in 1927 For 2 soprano voices, alto voice, and piano |
| Beschreibung: | 1 Online-Ressource (1 score (4 Seiten)) |
Internformat
MARC
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| 084 | |a MUS |q DE-12 |2 fid | ||
| 100 | 1 | |a Davies, Walford |d 1869-1941 |4 cmp | |
| 245 | 1 | 0 | |a A song of rest |b arranged as a trio, with pianoforte accompaniment |c words anonymous ; music by H. Walford Davies |
| 264 | 1 | |a [London, England] |b Novello & Company |c [1955] | |
| 264 | 4 | |c ©1955 | |
| 300 | |a 1 Online-Ressource (1 score (4 Seiten)) | ||
| 336 | |b ntm |2 rdacontent | ||
| 337 | |b c |2 rdamedia | ||
| 338 | |b cr |2 rdacarrier | ||
| 490 | 0 | |a Novello's octavo edition of trios, &c., for female voices |v trios 521 | |
| 500 | |a Title from title page (viewed March 27, 2019) | ||
| 500 | |a Written in 1927 | ||
| 500 | |a For 2 soprano voices, alto voice, and piano | ||
| 546 | |a English words | ||
| 650 | 4 | |a Vocal trios with piano | |
| 653 | 6 | |a Chamber music | |
| 653 | 6 | |a Arrangements (Music) | |
| 653 | 6 | |a Scores | |
| 856 | 4 | 0 | |u http://www.aspresolver.com/aspresolver.asp?SHM3;2382145 |x Verlag |z URL des Erstveröffentlichers |3 Volltext |
| 856 | 4 | 2 | |m DNB Datenaustausch |q application/pdf |u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=033815858&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
| 912 | |a ZDB-1-MOS | ||
| 999 | |a oai:aleph.bib-bvb.de:BVB01-033815858 | ||
| 382 | 1 | |a soprano voice |n 2 |a alto voice |n 1 |a piano |n 1 |s 4 |2 lcmpt | |
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Datensatz im Suchindex
| _version_ | 1804184361012035584 |
|---|---|
| adam_text | TABLE
OF
CONTENTS
ABSTRACT
.......................................................................................................................
XI
ZUSAMMENFASSUNG
..................................................................................................
XIII
1.
INTRODUCTION
............................................................................................................
1
1.1
THE
POPULATION
AND
GENETIC
DISORDERS
IN
YEMEN
.................................................
1
1.2
RARE
DISEASES
AND
MENDELIAN
DISORDERS
..............................................................
2
1.3
GENETIC
DIAGNOSIS
IN
THE
ERA
OF
NGS
...................................................................
3
1.3.1
TRADITIONAL
GENETIC
TESTING
METHODS
...................................................................
3
1.3.2
NEXT-GENERATION
SEQUENCING;
THE
GOLD
STANDARD
METHOD
FOR
DIAGNOSIS
OF
MENDELIAN
DISEASES
............................................................................................
4
1.4
MUSCULOSKELETAL
DISORDERS
.....................................................................................
5
1.4.1
INHERITED
MYOPATHIES
..........................................................................................
5
1.4.2
SKELETAL
DYSPLASIA
...............................................................................................
6
1.4.3
SPLIT
HAND
FOOT
MALFORMATION
..............................................................................
7
1.4.4
AN
OVERVIEW
OF
LIMB
DEVELOPMENT
IN
VERTEBRATE
................................................
8
1.4.4.1
THE
APICAL
ECTODERMAL
RIDGE
(AER)
...............................................................
8
1.4.4.2
HOX
GENES
IN
LIMB
DEVELOPMENT
...................................................................
10
1.4.4.3
WNT/P-CATENIN
SIGNALING
PATHWAY
IN
LIMB
DEVELOPMENT
...............................
11
1.4.5
LYMPHOID
ENHANCER
FACTOR
1
(LEF-1)
...............................................................
12
1.5
NEUROGENETIC
DISORDERS
.....................................................................................
14
1.5.1
EPIDEMIOLOGY
....................................................................................................
14
1.5.2
CLINICAL
PRESENTATION
........................................................................................
14
1.5.3
DIAGNOSIS
AND
MOLECULAR
TESTING
.....................................................................
15
1.5.4
GENE
THERAPY
APPROACHES
...............................................................................
15
1.5.5
THE
ROLE
OF
NDE1
IN
THE
PATHOGENESIS
OF
MICROCEPHALY
.................................
16
2.
AIMS
OF
THE
THESIS
...............................................................................................
18
3.
MATERIALS
AND
METHODS
.......................................................................................
19
3.1
PATIENTS
RECRUITMENT
AND
INFORMED
CONSENT
......................................................
19
3.2
PEDIGREE
DRAWING
AND
PATTERNS
OF
INHERITANCE
...................................................
20
3.3
DNA
COLLECTION,
EXTRACTION,
AND
QUANTIFICATION
..................................................
20
3.4
NEXT-GENERATION
SEQUENCING
................................................................................
21
3.4.1
WHOLE-EXOME
SEQUENCING
(WES)
AND
ANALYSIS
..............................................
21
3.4.2
MENDELIOME
SEQUENCING
...................................................................................
22
3.4.3
GENE
PANEL
SEQUENCING
................................................................................
22
3.5
SANGER
SEQUENCING
.............................................................................................
23
3.6
GENOME-WIDE
HOMOZYGOSITY
MAPPING
..............................................................
24
3.7
MOLECULAR
KARYOTYPING
WITH
CYTOSCAN
HD
ARRAY
...............................................
24
3.8
RNA
ISOLATION
AND
CDNA
SYNTHESIS
...................................................................
25
3.9
RNA
SEQUENCING
.................................................................................................
25
3.10
CHROMATIN
IMMUNOPRECIPITATION
(CHIP)
SEQUENCING
......................................
26
3.11
REAL-TIME
QUANTITATIVE
REVERSE
TRANSCRIPTION
PCR
(QRT-PCR)
.......................28
3.12
CELL
LINES
AND
CELL
CULTURE
..................................................................................
28
3.12.1
IMMORTALIZED
CELL
LINES
...................................................................................
28
3.12.2
PATIENT-DERIVED
DERMAL
FIBROBLASTS
...............................................................
28
3.13
CULTURE
MEDIA
AND
CONDITIONS
..........................................................................
29
3.14
CONSTRUCTION
OF
PLASMIDS
AND
SITE-DIRECTED
MUTAGENESIS
...............................
29
3.15
GST
PULL-DOWN
EXPERIMENT
...............................................................................
30
3.15.1
BACTERIAL
CULTURE
..............................................................................................30
3.15.2
TRANSFORMATION
OF
COMPETENT
BACTERIAL
CELLS
.................................................
30
3.15.3
EXPRESSION
AND
PURIFICATION
OF
GST
FUSION
PROTEINS
....................................
31
3.15.4
TRANSIENT
TRANSFECTION
AND
EXPRESSION
OF
GPP-TAGGED
CONSTRUCTS
..............
31
3.15.5
GST
PULL-DOWN
ASSAY
....................................................................................
32
3.16
MASS
SPECTROMETRY
ANALYSIS
.............................................................................
32
3.17
WESTERN
BLOT
ANALYSIS
......................................................................................
33
3.17.1
PREPARATION
OF
EUKARYOTIC
CELL
LYSATE
.............................................................
33
3.17.2
SODIUM
DODECYL
SULFATE-POLYACRYLAMIDE
GEL
ELECTROPHORESIS
(SDS-PAGE).34
3.17.3
PROTEIN
TRANSFER
TO
NITROCELLULOSE
MEMBRANE
AND
PROTEIN
DETECTION
...........
34
3.18
IMMUNOFLUORESCENCE
AND
CONFOCAL
MICROSCOPY
...............................................
35
3.18.1
SOLUTIONS
USED
FOR
IMMUNOFLUORESCENCE
STAINING
........................................
36
3.19
ANTIBODIES
..........................................................................................................
36
4.
RESULTS
.......................
38
4.1
OVERVIEW
AND
CLASSIFICATION
OF
THE
RECRUITED
FAMILIES
.......................................
38
4.2
MOLECULAR
GENETIC
AND
CYTOGENETIC
APPROACHES
IN
THE
DIAGNOSIS
OF
RARE
GENETIC
DISORDERS
.................................................................................................
39
4.3
NEUROGENETIC
DISORDERS
......................................................................................
41
4.4
MUSCULOSKELETAL
DISORDERS
..................................................................................
43
4.5
POTENTIAL
FOUNDER
MUTATIONS
...............................................................................
45
VIII
4.6
DUAL
MOLECULAR
DIAGNOSIS
OF
SPASTIC
PARAPLEGIA
AND
CONGENITAL
MUSCULAR
DYSTROPHY
..............................................................................................................
46
4.7
CONFIRMATION
OF
GENE-DISEASE
ASSOCIATION
........................................................
47
4.7.1
A
NOVEL
VARIANT
IN
NCAPD2
IS
CAUSING
MCPH
(THE
THIRD
REPORTED
FAMILY)
....
47
4.8
PHENOTYPIC
EXPANSION
.........................................................................................
47
4.8.1
CEP63:
EXPANDING
THE
PHENOTYPE
AND
CONFIRMING
DISEASE
ASSOCIATION
......
48
4.8.2
IDENTIFICATION
OF
NDE1
AS
A
DISEASE-ASSOCIATED
GENE
FOR
PRIMARY
MICRO
CEPHALY
WITHOUT
LISSENCEPHALY
...............................................................
49
4.8.2.1
PHENOTYPIC
DESCRIPTION
AND
BRAIN
MRI
FINDINGS
...........................................
49
4.8.2.2
WHOLE-EXOME
SEQUENCING
IDENTIFIED
A
DELETERIOUS
NDE1
VARIANT
............50
4.8.2.3
SUBCELLULAR
LOCALIZATION
AND
EXPRESSION
LEVEL
OF
MUTANT
NDE1
..................
51
4.9
LEF1
AS
A
NOVEL
CANDIDATE
GENE
FOR
SYNDROMIC
ECTRODACTYLY
............................
53
4.9.1
CLINICAL
AND
RADIOGRAPHIC
FINDINGS
...................................................................
53
4.9.2
WHOLE-EXOME
SEQUENCING
AND
SEGREGATION
ANALYSIS
...................................
54
4.9.3
THE
EFFECT
OF
P.M23DUP
ON
LEF-1
EXPRESSION
AND
LOCALIZATION
.....................58
4.9.4
THE
MET23DUP
VARIANT
SIGNIFICANTLY
REDUCED
THE
BINDING
AFFINITY
OF
LEF-1
FOR
BETA-CATENIN
................................................................................................60
4.9.5
MASS
SPECTROMETRY
..........................................................................................
61
4.9.6
RNA
SEQUENCING
.............................................................................................
62
4.9.7
CHLP-SEQUENCING
.............................................................................................
65
5.
DISCUSSION
...........................................................................................................67
5.1
GENETIC
DISORDERS
IN
YEMEN
...............................................................................
67
5.2
NGS
AS
A
GOLD
STANDARD
METHOD
FOR
THE
DIAGNOSIS
OF
GENETIC
DISORDERS
........
68
5.3
THE
QUEST
FOR
FOUNDER
MUTATIONS
........................................................................69
5.4
DUAL
MOLECULAR
DIAGNOSIS:
EASY
TO
BE
OVERLOOKED
...........................................
70
5.5
SECKEL
SYNDROME
TYPE
6:
REPORTING
A
THIRD
FAMILY
AND
EXPANDING
THE
CLINICAL
PHENOTYPE
..............................................................................................70
5.6
A
TRUNCATING
NDE1
VARIANT
CAUSING
AUTOSOMAL
RECESSIVE
PRIMARY
MICRO
CEPHALY
WITHOUT
LISSENCEPHALY
.......................................................................
71
5.7
LEF1,
A
NOVEL
GENE
ASSOCIATED
WITH
ECTRODACTYLY
ECTODERMAL
DYSPLASIA
WITHOUT
CLEFT
LIP/PALATE
.........................................................................................
73
6
CONCLUSION
AND
OUTLOOK
......................................................................................
77
7
REFERENCES
............................................................................................................
79
IX
8
APPENDICES
........................................................................................................
97
8.1
APPENDIX
1
..........................................................................................................
97
8.2
APPENDIX
2
..........................................................................................................
99
8.3
ABBREVIATIONS
.....................................................................................................
100
8.4
LIST
OF
PUBLICATIONS
.............................................................................................
103
8.5
LIST
OF
FIGURES
....................................................................................................
104
8.6
LIST
OF
TABLES
......................................................................................................
105
8.7
CURRICULUM
VITAE
(CV)/
LEBENSLAUF
...................................................................
106
ERKLARUNG/
DECLARATION
........................................................................................
108
X
|
| adam_txt |
TABLE
OF
CONTENTS
ABSTRACT
.
XI
ZUSAMMENFASSUNG
.
XIII
1.
INTRODUCTION
.
1
1.1
THE
POPULATION
AND
GENETIC
DISORDERS
IN
YEMEN
.
1
1.2
RARE
DISEASES
AND
MENDELIAN
DISORDERS
.
2
1.3
GENETIC
DIAGNOSIS
IN
THE
ERA
OF
NGS
.
3
1.3.1
TRADITIONAL
GENETIC
TESTING
METHODS
.
3
1.3.2
NEXT-GENERATION
SEQUENCING;
THE
GOLD
STANDARD
METHOD
FOR
DIAGNOSIS
OF
MENDELIAN
DISEASES
.
4
1.4
MUSCULOSKELETAL
DISORDERS
.
5
1.4.1
INHERITED
MYOPATHIES
.
5
1.4.2
SKELETAL
DYSPLASIA
.
6
1.4.3
SPLIT
HAND
FOOT
MALFORMATION
.
7
1.4.4
AN
OVERVIEW
OF
LIMB
DEVELOPMENT
IN
VERTEBRATE
.
8
1.4.4.1
THE
APICAL
ECTODERMAL
RIDGE
(AER)
.
8
1.4.4.2
HOX
GENES
IN
LIMB
DEVELOPMENT
.
10
1.4.4.3
WNT/P-CATENIN
SIGNALING
PATHWAY
IN
LIMB
DEVELOPMENT
.
11
1.4.5
LYMPHOID
ENHANCER
FACTOR
1
(LEF-1)
.
12
1.5
NEUROGENETIC
DISORDERS
.
14
1.5.1
EPIDEMIOLOGY
.
14
1.5.2
CLINICAL
PRESENTATION
.
14
1.5.3
DIAGNOSIS
AND
MOLECULAR
TESTING
.
15
1.5.4
GENE
THERAPY
APPROACHES
.
15
1.5.5
THE
ROLE
OF
NDE1
IN
THE
PATHOGENESIS
OF
MICROCEPHALY
.
16
2.
AIMS
OF
THE
THESIS
.
18
3.
MATERIALS
AND
METHODS
.
19
3.1
PATIENTS
RECRUITMENT
AND
INFORMED
CONSENT
.
19
3.2
PEDIGREE
DRAWING
AND
PATTERNS
OF
INHERITANCE
.
20
3.3
DNA
COLLECTION,
EXTRACTION,
AND
QUANTIFICATION
.
20
3.4
NEXT-GENERATION
SEQUENCING
.
21
3.4.1
WHOLE-EXOME
SEQUENCING
(WES)
AND
ANALYSIS
.
21
3.4.2
MENDELIOME
SEQUENCING
.
22
3.4.3
GENE
PANEL
SEQUENCING
.
22
3.5
SANGER
SEQUENCING
.
23
3.6
GENOME-WIDE
HOMOZYGOSITY
MAPPING
.
24
3.7
MOLECULAR
KARYOTYPING
WITH
CYTOSCAN
HD
ARRAY
.
24
3.8
RNA
ISOLATION
AND
CDNA
SYNTHESIS
.
25
3.9
RNA
SEQUENCING
.
25
3.10
CHROMATIN
IMMUNOPRECIPITATION
(CHIP)
SEQUENCING
.
26
3.11
REAL-TIME
QUANTITATIVE
REVERSE
TRANSCRIPTION
PCR
(QRT-PCR)
.28
3.12
CELL
LINES
AND
CELL
CULTURE
.
28
3.12.1
IMMORTALIZED
CELL
LINES
.
28
3.12.2
PATIENT-DERIVED
DERMAL
FIBROBLASTS
.
28
3.13
CULTURE
MEDIA
AND
CONDITIONS
.
29
3.14
CONSTRUCTION
OF
PLASMIDS
AND
SITE-DIRECTED
MUTAGENESIS
.
29
3.15
GST
PULL-DOWN
EXPERIMENT
.
30
3.15.1
BACTERIAL
CULTURE
.30
3.15.2
TRANSFORMATION
OF
COMPETENT
BACTERIAL
CELLS
.
30
3.15.3
EXPRESSION
AND
PURIFICATION
OF
GST
FUSION
PROTEINS
.
31
3.15.4
TRANSIENT
TRANSFECTION
AND
EXPRESSION
OF
GPP-TAGGED
CONSTRUCTS
.
31
3.15.5
GST
PULL-DOWN
ASSAY
.
32
3.16
MASS
SPECTROMETRY
ANALYSIS
.
32
3.17
WESTERN
BLOT
ANALYSIS
.
33
3.17.1
PREPARATION
OF
EUKARYOTIC
CELL
LYSATE
.
33
3.17.2
SODIUM
DODECYL
SULFATE-POLYACRYLAMIDE
GEL
ELECTROPHORESIS
(SDS-PAGE).34
3.17.3
PROTEIN
TRANSFER
TO
NITROCELLULOSE
MEMBRANE
AND
PROTEIN
DETECTION
.
34
3.18
IMMUNOFLUORESCENCE
AND
CONFOCAL
MICROSCOPY
.
35
3.18.1
SOLUTIONS
USED
FOR
IMMUNOFLUORESCENCE
STAINING
.
36
3.19
ANTIBODIES
.
36
4.
RESULTS
.
38
4.1
OVERVIEW
AND
CLASSIFICATION
OF
THE
RECRUITED
FAMILIES
.
38
4.2
MOLECULAR
GENETIC
AND
CYTOGENETIC
APPROACHES
IN
THE
DIAGNOSIS
OF
RARE
GENETIC
DISORDERS
.
39
4.3
NEUROGENETIC
DISORDERS
.
41
4.4
MUSCULOSKELETAL
DISORDERS
.
43
4.5
POTENTIAL
FOUNDER
MUTATIONS
.
45
VIII
4.6
DUAL
MOLECULAR
DIAGNOSIS
OF
SPASTIC
PARAPLEGIA
AND
CONGENITAL
MUSCULAR
DYSTROPHY
.
46
4.7
CONFIRMATION
OF
GENE-DISEASE
ASSOCIATION
.
47
4.7.1
A
NOVEL
VARIANT
IN
NCAPD2
IS
CAUSING
MCPH
(THE
THIRD
REPORTED
FAMILY)
.
47
4.8
PHENOTYPIC
EXPANSION
.
47
4.8.1
CEP63:
EXPANDING
THE
PHENOTYPE
AND
CONFIRMING
DISEASE
ASSOCIATION
.
48
4.8.2
IDENTIFICATION
OF
NDE1
AS
A
DISEASE-ASSOCIATED
GENE
FOR
PRIMARY
MICRO
CEPHALY
WITHOUT
LISSENCEPHALY
.
49
4.8.2.1
PHENOTYPIC
DESCRIPTION
AND
BRAIN
MRI
FINDINGS
.
49
4.8.2.2
WHOLE-EXOME
SEQUENCING
IDENTIFIED
A
DELETERIOUS
NDE1
VARIANT
.50
4.8.2.3
SUBCELLULAR
LOCALIZATION
AND
EXPRESSION
LEVEL
OF
MUTANT
NDE1
.
51
4.9
LEF1
AS
A
NOVEL
CANDIDATE
GENE
FOR
SYNDROMIC
ECTRODACTYLY
.
53
4.9.1
CLINICAL
AND
RADIOGRAPHIC
FINDINGS
.
53
4.9.2
WHOLE-EXOME
SEQUENCING
AND
SEGREGATION
ANALYSIS
.
54
4.9.3
THE
EFFECT
OF
P.M23DUP
ON
LEF-1
EXPRESSION
AND
LOCALIZATION
.58
4.9.4
THE
MET23DUP
VARIANT
SIGNIFICANTLY
REDUCED
THE
BINDING
AFFINITY
OF
LEF-1
FOR
BETA-CATENIN
.60
4.9.5
MASS
SPECTROMETRY
.
61
4.9.6
RNA
SEQUENCING
.
62
4.9.7
CHLP-SEQUENCING
.
65
5.
DISCUSSION
.67
5.1
GENETIC
DISORDERS
IN
YEMEN
.
67
5.2
NGS
AS
A
GOLD
STANDARD
METHOD
FOR
THE
DIAGNOSIS
OF
GENETIC
DISORDERS
.
68
5.3
THE
QUEST
FOR
FOUNDER
MUTATIONS
.69
5.4
DUAL
MOLECULAR
DIAGNOSIS:
EASY
TO
BE
OVERLOOKED
.
70
5.5
SECKEL
SYNDROME
TYPE
6:
REPORTING
A
THIRD
FAMILY
AND
EXPANDING
THE
CLINICAL
PHENOTYPE
.70
5.6
A
TRUNCATING
NDE1
VARIANT
CAUSING
AUTOSOMAL
RECESSIVE
PRIMARY
MICRO
CEPHALY
WITHOUT
LISSENCEPHALY
.
71
5.7
LEF1,
A
NOVEL
GENE
ASSOCIATED
WITH
ECTRODACTYLY
ECTODERMAL
DYSPLASIA
WITHOUT
CLEFT
LIP/PALATE
.
73
6
CONCLUSION
AND
OUTLOOK
.
77
7
REFERENCES
.
79
IX
8
APPENDICES
.
97
8.1
APPENDIX
1
.
97
8.2
APPENDIX
2
.
99
8.3
ABBREVIATIONS
.
100
8.4
LIST
OF
PUBLICATIONS
.
103
8.5
LIST
OF
FIGURES
.
104
8.6
LIST
OF
TABLES
.
105
8.7
CURRICULUM
VITAE
(CV)/
LEBENSLAUF
.
106
ERKLARUNG/
DECLARATION
.
108
X |
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| author | Davies, Walford 1869-1941 |
| author_facet | Davies, Walford 1869-1941 |
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| format | Electronic Musical Score Book |
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| id | DE-604.BV048437588 |
| illustrated | Not Illustrated |
| index_date | 2024-07-03T20:28:26Z |
| indexdate | 2024-07-10T09:38:07Z |
| institution | BVB |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-033815858 |
| oclc_num | 1237665485 |
| open_access_boolean | |
| owner | DE-12 |
| owner_facet | DE-12 |
| physical | 1 Online-Ressource (1 score (4 Seiten)) |
| psigel | ZDB-1-MOS |
| publishDate | 1955 |
| publishDateSearch | 1955 |
| publishDateSort | 1955 |
| publisher | Novello & Company |
| record_format | marc |
| series2 | Novello's octavo edition of trios, &c., for female voices |
| spelling | Davies, Walford 1869-1941 cmp A song of rest arranged as a trio, with pianoforte accompaniment words anonymous ; music by H. Walford Davies [London, England] Novello & Company [1955] ©1955 1 Online-Ressource (1 score (4 Seiten)) ntm rdacontent c rdamedia cr rdacarrier Novello's octavo edition of trios, &c., for female voices trios 521 Title from title page (viewed March 27, 2019) Written in 1927 For 2 soprano voices, alto voice, and piano English words Vocal trios with piano Chamber music Arrangements (Music) Scores http://www.aspresolver.com/aspresolver.asp?SHM3;2382145 Verlag URL des Erstveröffentlichers Volltext DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=033815858&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis soprano voice 2 alto voice 1 piano 1 4 lcmpt |
| spellingShingle | Davies, Walford 1869-1941 A song of rest arranged as a trio, with pianoforte accompaniment Vocal trios with piano |
| title | A song of rest arranged as a trio, with pianoforte accompaniment |
| title_auth | A song of rest arranged as a trio, with pianoforte accompaniment |
| title_exact_search | A song of rest arranged as a trio, with pianoforte accompaniment |
| title_exact_search_txtP | A song of rest arranged as a trio, with pianoforte accompaniment |
| title_full | A song of rest arranged as a trio, with pianoforte accompaniment words anonymous ; music by H. Walford Davies |
| title_fullStr | A song of rest arranged as a trio, with pianoforte accompaniment words anonymous ; music by H. Walford Davies |
| title_full_unstemmed | A song of rest arranged as a trio, with pianoforte accompaniment words anonymous ; music by H. Walford Davies |
| title_short | A song of rest |
| title_sort | a song of rest arranged as a trio with pianoforte accompaniment |
| title_sub | arranged as a trio, with pianoforte accompaniment |
| topic | Vocal trios with piano |
| topic_facet | Vocal trios with piano |
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