Deletion 4q21/4q22 syndrome: Two patients with de novo 4q21.3q23 and 4q13.2q23 deletions

American Journal of Medical Genetics

Volumn 69, Issue 4, 1997, Pages 400-405

  Nowaczyk, M J M ^a,b   Teshima, I E ^a   Siegel Bartelt, J ^a   Clarke, J T R ^a  

^a UNIVERSITY OF TORONTO   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

alphafetoprotein; chromosome deletion; human chromosome 4; hydrocephalus; megalencephaly

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 4Q; CLINICAL FEATURE; HUMAN; HYDROCEPHALUS; INFANT; INTERSTITIAL CHROMOSOME DELETION; MALE; PRIORITY JOURNAL; SYNDROME DELINEATION;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; FATAL OUTCOME; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MALE; SKULL; SYNDROME; TOMOGRAPHY SCANNERS, X-RAY COMPUTED;

EID: 0030908305     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970414)69:4<400::AID-AJMG12>3.0.CO;2-R     Document Type: Article

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