Holoprosencephaly: An update on cytogenetic abnormalities

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 154, Issue 1, 2010, Pages 86-92

  Bendavid, Claude ^f   Dupé, Valérie ^a,b   Rochard, Lucie ^c   Gicquel, Isabelle ^c   Dubourg, Christèle ^d,e   David, Véronique ^d,e  

^a INSERM   (France)

^b UNIVERSITÉ DE RENNES 1   (France)

^c UNIVERSITÉ DE RENNES 1   (France)

^d CNRS   (France)

^e PONTCHAILLOU UNIVERSITY HOSPITAL   (France)

^f NONE

Author keywords

Array CGH; Candidate loci molecular diagnosis; Holoprosencephaly; HPE; MLPA

Indexed keywords

CHROMOSOME 14Q; CHROMOSOME 21Q; CHROMOSOME 2Q; COMPARATIVE GENOMIC HYBRIDIZATION; GENE DELETION; GENE IDENTIFICATION; GENE LOCATION; GENE REARRANGEMENT; HOLOPROSENCEPHALY; HUMAN; KARYOTYPING; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; PRIORITY JOURNAL; REVIEW;

CHROMOSOME ABERRATIONS; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; HOLOPROSENCEPHALY; HUMANS; KARYOTYPING; MICROARRAY ANALYSIS; MOLECULAR DIAGNOSTIC TECHNIQUES; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 76149091554     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.30250     Document Type: Review

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