Duplication of 7p21.2→pter Due to maternal 7p;21q translocation: Implications for critical segment assignment in the 7p duplication syndrome

American Journal of Medical Genetics

Volumn 86, Issue 4, 1999, Pages 305-311

  Cai, Tao ^a   Yu, Ping ^b   Tagle, Danilo A ^b   Xia, Jiahui ^c  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

^c NONE

Author keywords

7p duplication; Craniofacial development; Mental retardation; Syndrome

Indexed keywords

ANTERIOR FONTANEL; ARTICLE; BRACHYCEPHALY; CHROMOSOME 21Q; CHROMOSOME 7P; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; CRANIOFACIAL DEVELOPMENT; HUMAN; HYPERTELORISM; MENTAL DEFICIENCY; MUSCLE HYPOTONIA; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 7; CRANIOFACIAL ABNORMALITIES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MENTAL RETARDATION; PHENOTYPE; SYNDROME; TRANSLOCATION, GENETIC;

EID: 0032872667     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19991008)86:4<305::AID-AJMG1>3.0.CO;2-B     Document Type: Article

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