Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)]

American Journal of Medical Genetics

Volumn 128 A, Issue 1, 2004, Pages 72-77

  Yatsenko, Svetlana A ^a   Sahoo, Trilochan ^a   Rosenkranz, Melinda ^a   Mendoza Londono, Roberto ^a   Naeem, Rizwan ^a,b   Scaglia, Fernando ^a,b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b TEXAS CHILDREN S HOSPITAL   (United States)

Author keywords

Der(X); Late replication; Monosomy Xq; Trisomy 1q; X inactivation

Indexed keywords

ARTICLE; AUTOSOME MOSAICISM; CASE REPORT; CHROMOSOME 1Q; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CHROMOSOME REPLICATION; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION X; CHROMOSOME XQ; CONGENITAL HEART MALFORMATION; DERIVATIVE X CHROMOSOME; DEVELOPMENTAL DISORDER; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; INFANT; MONOSOMY X; MONOSOMY XQ; PHENOTYPE; PRIORITY JOURNAL; TRISOMY; TRISOMY 1Q; UNBALANCED TRANSLOCATION; UROGENITAL TRACT MALFORMATION; X CHROMOSOME INACTIVATION;

EID: 3042724653     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30094     Document Type: Article

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