Terminal deletion of chromosome 10q: Clinical features and literature review

Pediatrics International

Volumn 41, Issue 5, 1999, Pages 565-567

  Tanabe, Saori ^a,b   Akiba, Tomoharu ^a,c   Katoh, Mitsuhiro ^b   Satoh, Tetsuo ^a  

^a Nagai City Hospital   (Japan)

^b YAMAGATA UNIVERSITY   (Japan)

^c Yamagata City Hospital Saiseikan   (Japan)

Author keywords

Chromosome 10q; Deletion

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 10Q; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; GROWTH RETARDATION; HUMAN; INFANT; MALE; PRIORITY JOURNAL; UROGENITAL TRACT MALFORMATION;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 10; HUMANS; INFANT, NEWBORN; MALE; PHENOTYPE;

EID: 0032885399     PISSN: 13288067     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1442-200x.1999.01105.x     Document Type: Article

References (11)

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