Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation

Journal of Medical Genetics

Volumn 33, Issue 11, 1996, Pages 906-911

  Joseph, Maries ^a   Cantú, Eduardo S ^a   Pai, G Shashidhar ^a   Willi, Steven M ^a   Papenhausen, Peter R ^c   Weiss, Lester ^b  

^a MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

^b HENRY FORD HOSPITAL   (United States)

^c Henry Ford Hospital ^*

Author keywords

FISH; Pseudoautosomal genes; Short stature; X; Y translocation

Indexed keywords

COLONY STIMULATING FACTOR; INTERLEUKIN 3 RECEPTOR;

AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME TRANSLOCATION X; CHROMOSOME XP; CHROMOSOME YP; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOCUS; GROWTH RATE; GROWTH RETARDATION; HUMAN; HUMAN CELL; INFANT; NEWBORN; PRESCHOOL CHILD; PRIORITY JOURNAL; SHORT STATURE; TURNER SYNDROME;

RICKETTSIA SP. PAR;

EID: 0029845509     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.33.11.906     Document Type: Article

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