Familial occurrence of a del(Xp-) chromosome: Pitfall in karyotype/phenotype correlation [2]

American Journal of Medical Genetics

Volumn 80, Issue 4, 1998, Pages 436-438

  Soyke, A ^a   Stumm, M ^a   Krebs, P ^a   Kloos, D U ^a   Wieacker, P ^a   Elsner, J ^a   Mohnike, K ^a  

^a UNIVERSITY HOSPITAL MAGDEBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL INHERITANCE; CHROMOSOME DELETION; CHROMOSOME MOSAICISM; DIAGNOSTIC ACCURACY; GENETIC SUSCEPTIBILITY; HUMAN; KARYOTYPE 45,X; KARYOTYPING; LETTER; PHENOTYPE; PRIORITY JOURNAL; RISK ASSESSMENT;

ADOLESCENT; ADULT; CHILD; CHROMOSOME DELETION; FAMILY HEALTH; FEMALE; HUMANS; KARYOTYPING; MALE; PEDIGREE; PHENOTYPE; TURNER SYNDROME; X CHROMOSOME;

EID: 0031772325     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19981204)80:4<436::AID-AJMG26>3.0.CO;2-4     Document Type: Letter

References (17)