Clinical and molecular analysis of five inv dup(15) patients.

European journal of human genetics : EJHG

Volumn 1, Issue 1, 1993, Pages 37-50

  Robinson, W P ^a   Binkert, F ^a   Gine R ^a   Vazquez, C ^a   Muller W ^a   Rosenkranz, W ^a   Schinzel, A ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ANEUPLOIDY; ARTICLE; CASE REPORT; CHROMOSOME 15; CHROMOSOME ABERRATION; CHROMOSOME DISORDER; CHROMOSOME INVERSION; EPILEPSY; FEMALE; GENETICS; HUMAN; IN SITU HYBRIDIZATION; INFANT; KARYOTYPING; MALE; MENTAL DEFICIENCY; MOSAICISM; MOTHER; MULTIGENE FAMILY; MULTIPLE MALFORMATION SYNDROME; NEWBORN;

ABNORMALITIES, MULTIPLE; ALLELES; ANEUPLOIDY; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 15; EPILEPSY; FEMALE; HUMANS; IN SITU HYBRIDIZATION; INFANT; INFANT, NEWBORN; INVERSION, CHROMOSOME; KARYOTYPING; MALE; MENTAL RETARDATION; MOSAICISM; MOTHERS; MULTIGENE FAMILY;

EID: 0027792161     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472386     Document Type: Article

References (0)