The parental origin of the single X chromosome in Turner syndrome: Lack of correlation with parental age or clinical phenotype

American Journal of Human Genetics

Volumn 48, Issue 4, 1991, Pages 682-686

  Mathur, A ^a   Stekol, L ^a   Schatz, D ^a   MacLaren, N K ^a   Scott, M L ^a   Lippe, B ^a  

^a UCLA MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; ARTICLE; CHILD; CHROMOSOME LOSS; CLINICAL ARTICLE; DNA PROBE; FEMALE; HUMAN; MEIOSIS; MONOSOMY X; PARENT; PRIORITY JOURNAL; TURNER SYNDROME;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; HUMAN; MALE; PATERNAL AGE; PHENOTYPE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T; TURNER SYNDROME; X CHROMOSOME;

EID: 0025763762     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)