Chromosome 1p36 deletions: The clinical phenotype and molecular characterization of a common newly delineated syndrome

American Journal of Human Genetics

Volumn 61, Issue 3, 1997, Pages 642-650

  Shapira, Stuart K ^a   McCaskill, Christopher ^a   Northrup, Hope ^b   Spikes, Aimee S ^a   Elder, F F B ^b   Sutton, V Reid ^a   Korenberg, Julie R ^c   Greenberg, Frank ^d   Shaffer, Lisa G ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^c CEDARS SINAI MEDICAL CENTER   (United States)

^d NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 1P; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; CYTOGENETICS; DNA POLYMORPHISM; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH RETARDATION; HUMAN; MENTAL DEFICIENCY; MENTAL RETARDATION MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL; SYNDROME DELINEATION;

EID: 0030870848     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/515520     Document Type: Article

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