Del(X)(p21.2) in a mother and two daughters with variable ovarian function

Clinical Genetics

Volumn 52, Issue 4, 1997, Pages 235-239

  Zinn, Andrew R ^a,d   Ouyang, Bing ^a   Ross, Judith L ^b   Varma, Surendra ^c   Bourgeois, Michael ^c   Tonk, Vijay ^c  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b THOMAS JEFFERSON UNIVERSITY   (United States)

^c TEXAS TECH UNIVERSITY   (United States)

^d UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

Chromosome deletion; Gonadal dysgenesis; Monosomy; Ovarian failure; Premature; Turner syndrome; X chromosome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CHROMOSOME DELETION X; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; MOSAICISM; OVARY INSUFFICIENCY; PRIORITY JOURNAL; TURNER SYNDROME;

EID: 0030825969     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1997.tb02554.x     Document Type: Article

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