An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21

American Journal of Human Genetics

Volumn 70, Issue 4, 2002, Pages 1028-1033

  Piao, Xianhua ^a,b   Basel Vanagaite, Lina ^c   Straussberg, Rachel ^d   Grant, P Ellen ^e   Pugh, Elizabeth W ^h   Doheny, Kim ^h   Doan, Betty ^f,h   Hong, Susan E ^a   Shugart, Yin Yao ^f,h   Walsh, Christopher A ^g  

^a HARVARD MEDICAL SCHOOL   (United States)

^b Children s Hospital   (United States)

^c RABIN MEDICAL CENTER   (Israel)

^d SCHNEIDER CHILDREN S MEDICAL CENTER OF ISRAEL   (Israel)

^e MASSACHUSETTS GENERAL HOSPITAL   (United States)

^f JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

^g HARVARD INSTITUTES OF MEDICINE   (United States)

^h JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BRAIN MAPPING; BRAIN RADIOGRAPHY; CHROMOSOME 16Q; CHROMOSOME MAP; CLINICAL EXAMINATION; CONVERGENT STRABISMUS; DEVELOPMENTAL DISORDER; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; HAPLOTYPE; HUMAN; MENTAL DEFICIENCY; MICROGYRIA; MICROSCOPY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; RADIODIAGNOSIS;

EID: 18344389160     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/339552     Document Type: Article

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