Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
about
Angelman Syndrome due to familial translocation: unexpected additional results characterized by Microarray-based Comparative Genomic Hybridization.Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients.Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome "tiling path" BAC array in a girl with heart defect, cleft palate, and developmental delay.15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization.An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype.
P2860
Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年學術文章
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2004年學術文章
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2004年學術文章
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name
Prader-Willi syndrome with an ...... alanced translocation t(4;15).
@ast
Prader-Willi syndrome with an ...... alanced translocation t(4;15).
@en
type
label
Prader-Willi syndrome with an ...... alanced translocation t(4;15).
@ast
Prader-Willi syndrome with an ...... alanced translocation t(4;15).
@en
prefLabel
Prader-Willi syndrome with an ...... alanced translocation t(4;15).
@ast
Prader-Willi syndrome with an ...... alanced translocation t(4;15).
@en
P2093
P1433
P1476
Prader-Willi syndrome with an ...... alanced translocation t(4;15).
@en
P2093
Celia P Koiffmann
Graziela M P Lopes
Monica C Varela
P304
P356
10.1016/J.ANNGEN.2004.01.003
P577
2004-07-01T00:00:00Z