Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26)

American Journal of Medical Genetics

Volumn 102, Issue 1, 2001, Pages 81-85

  Reinehr, Thomas ^a   Jauch, Anna ^b   Zoll, Barbara ^c   Engel, Ute ^a   Bartels, Iris ^a   Andler, Werner ^b  

^a UNIVERSITY OF WITTEN HERDECKE   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

Add(X)(p22.3); Short stature; SHOX

Indexed keywords

HUMAN GROWTH HORMONE; STERYL SULFATASE;

ADULT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME BAND; CHROMOSOME MOSAICISM; CHROMOSOME XP; CHROMOSOME XQ; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HOMEOBOX; HUMAN; KARYOTYPE; METAPHASE; MONOSOMY; MOTHER; PRIORITY JOURNAL; SHORT STATURE; TRISOMY;

ADULT; ARYLSULFATASES; CHILD; CHROMOSOME BANDING; CHROMOSOME PAINTING; FAMILY HEALTH; FEMALE; GROWTH DISORDERS; HOMEODOMAIN PROTEINS; HUMANS; KARYOTYPING; STERYL-SULFATASE; TRANSLOCATION, GENETIC; X CHROMOSOME;

EID: 0035934016     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010722)102:1<81::AID-AJMG1375>3.0.CO;2-V     Document Type: Article

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