Co-occurrence of Prader-Willi and Sotos syndromes

American Journal of Medical Genetics, Part A

Volumn 152, Issue 8, 2010, Pages 2103-2109

  Okamoto, Nobuhiko ^a   Akimaru, Noriko ^a   Matsuda, Keiko ^a   Suzuki, Yasuhiro ^a   Shimojima, Keiko ^b   Yamamoto, Toshiyuki ^b  

^a RESEARCH INSTITUTE FOR MATERNAL AND CHILD HEALTH   (Japan)

^b TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

Author keywords

aCGH; Prader Willi syndrome; Sotos syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 15Q; CHROMOSOME 5Q; CHROMOSOME ABERRATION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART MALFORMATION; DEVELOPMENTAL DISORDER; DISEASE SEVERITY; FOREHEAD; GENOMICS; HUMAN; INCIDENTAL FINDING; MACROCEPHALY; MALE; MICROARRAY ANALYSIS; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SOTOS SYNDROME;

ADOLESCENT; CHROMOSOMES, HUMAN, PAIR 15; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISABILITIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PRADER-WILLI SYNDROME; SYNDROME;

EID: 77955296389     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33544     Document Type: Article

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