Molecular cytogenetic analysis of a de novo 5q31q33 deletion associated multiple congenital anomalies: Case report

American Journal of Medical Genetics

Volumn 82, Issue 2, 1999, Pages 143-145

  Kramer, Ralph L ^a   Feldman, Baruch ^a   Ebrahim, Salah A D ^a,b   Kasperski, Stefanie B ^a   Johnson, Mark P ^a   Evans, Mark I ^a,c  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b DETROIT MEDICAL CENTER   (United States)

^c WAYNE STATE UNIVERSITY   (United States)

Author keywords

Congenital anomalies; Interstitial deletion of 5q; Prenatal diagnosis

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 5Q; CHROMOSOME DELETION; CYTOGENETICS; FETUS ECHOGRAPHY; HUMAN; MALE; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ABNORMALITIES; ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 5; FEMALE; HUMANS; KARYOTYPING; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 0033556373     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990115)82:2<143::AID-AJMG8>3.0.CO;2-V     Document Type: Article

References (13)

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