Holoprosencephaly, hypertelorism, and ectrodactyly in a boy with an apparently balanced de novo t(2;4)(q14.2;q35)

American Journal of Medical Genetics

Volumn 90, Issue 5, 2000, Pages 423-426

  Corona Rivera, Alfredo ^a,b   Corona Rivera, J Román ^a,b   Bobadilla Morales, Lucina ^a   García Cobian, Teresa A ^a   Corona Rivera, Enrique ^a  

^a UNIVERSITY OF GUADALAJARA   (Mexico)

^b HOSPITAL CIVIL DE GUADALAJARA FRAY ANTONIO ALCALDE   (Mexico)

Author keywords

Balanced translocations; Chromosome 2q14.2; Chromosome 4q35; Cryptic translocations; Syndactyly

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOMAL LOCALIZATION; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; ECTRODACTYLY; FLUORESCENCE; HOLOPROSENCEPHALY; HUMAN; HYPERTELORISM; IN SITU HYBRIDIZATION; MALE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 4; FOOT DEFORMITIES, CONGENITAL; HOLOPROSENCEPHALY; HUMANS; HYPERTELORISM; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; TRANSLOCATION, GENETIC;

EID: 0034723719     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000228)90:5<423::AID-AJMG12>3.0.CO;2-K     Document Type: Article

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