Uniparental disomy as a mechanism for human genetic disease

American Journal of Human Genetics

Volumn 42, Issue 2, 1988, Pages 217-226

  Spence, J E ^a   Perciaccante, R G ^a   Greig, G M ^a   Willard, H F ^a   Ledbetter, D H ^a   Fielding Hejtmancik, ^a   Pollack, M S ^a   O'Brien, W E ^a   Beaudet, A L ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; BIOLOGICAL MODEL; CASE REPORT; CHILD; CYSTIC FIBROSIS; CYTOLOGY; DISOMY; DNA PROBE; FEMALE; FERTILIZATION; GAMETE; GENETIC DISORDER; GENETIC ENGINEERING; GENETIC MODEL; HEREDITY; HOMOZYGOSITY; HUMAN;

ADOLESCENT; CASE REPORT; CHROMOSOMES, HUMAN, PAIR 7; CYSTIC FIBROSIS; FEMALE; GENETIC MARKERS; GROWTH DISORDERS; HUMAN; NONDISJUNCTION, GENETIC; PARENTS; PEDIGREE; PHENOTYPE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0023897290     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)