A unique genomic sequence in the Wolf-Hirschhorn syndrome [WHS] region of humans is conserved in the great apes

Genetica

Volumn 98, Issue 2, 1996, Pages 217-219

  Tarzami, Sima T ^a  

^a LONG ISLAND COLLEGE HOSPITAL   (United States)

Author keywords

Ape chromosome 3; Chimpanzee; Gorilla; Human chromosome 4; Orangutan; Wolf hirschhorn syndrome

Indexed keywords

ANIMAL; ANTHROPOIDEA; ARTICLE; CHROMOSOME 4; CHROMOSOME DELETION; CHROMOSOME MAP; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC VARIABILITY; GENETICS; GORILLA; HOMINID; HUMAN; MULTIPLE MALFORMATION SYNDROME; PAN TROGLODYTES;

ABNORMALITIES, MULTIPLE; ANIMALS; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 4; GORILLA GORILLA; HOMINIDAE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PAN TROGLODYTES; PONGO PYGMAEUS; VARIATION (GENETICS);

EID: 0030267978     PISSN: 00166707     EISSN: None     Source Type: Journal    
DOI: 10.1007/bf00121370     Document Type: Article

References (1)

1. Anvret, M., M. Nordenskjold, L. Stolpe, L. Johansson & K. Brondum-Nielsen, 1991. Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the 'critical segment' towards the telomere. Hum. Genet. 86: 481-483.