De novo interstitial proximal deletion of 14q and prenatal diagnosis of holoprosencephaly [3]

Prenatal Diagnosis

Volumn 16, Issue 11, 1996, Pages 1059-1060

  Bruyere, H ^a   Favre, B ^a   Douvier, S ^a   Nivelon Chevalier, A ^a   Mugneret, F ^a  

^a UNIVERSITÉ DE BOURGOGNE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; CHROMOSOME 14Q; CHROMOSOME ABERRATION; CLINICAL FEATURE; FEMALE; GENE DELETION; HOLOPROSENCEPHALY; HUMAN; LETTER; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ADULT; CHROMOSOMES, HUMAN, PAIR 14; FEMALE; GENE DELETION; HOLOPROSENCEPHALY; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 0029846092     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199611)16:11<1059::AID-PD993>3.0.CO;2-Z     Document Type: Letter

References (0)