Clinical significance of the parental origin of the X chromosome in Turner syndrome

Journal of Clinical Endocrinology and Metabolism

Volumn 92, Issue 3, 2007, Pages 846-852

  Sagi, Liora ^a   Zuckerman Levin, Nehama ^a   Gawlik, Aneta ^b   Ghizzoni, Lucia ^c   Buyukgebiz, Atilla ^d   Rakover, Yardena ^e   Bistritzer, Tzvi ^f   Admoni, Osnat ^e   Vottero, Alessandra ^c   Baruch, Oshrat ^a   Fares, Fuad ^g,h   Malecka Tendera, Ewa ^b   Hochberg, Ze'ev ^a,h  

^a MEYER CHILDREN S HOSPITAL   (Israel)

^b MEDICAL UNIVERSITY OF SILESIA   (Poland)

^c UNIVERSITY OF PARMA   (Italy)

^d Department of Pediatrics   (Turkey)

^e HAEMEK MEDICAL CENTER   (Israel)

^f ASSAF HAROFEH MEDICAL CENTER   (Israel)

^g CARMEL MEDICAL CENTER   (Israel)

^h TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR; GROWTH HORMONE; LOW DENSITY LIPOPROTEIN CHOLESTEROL;

ADOLESCENT; ADULT; ANTHROPOMETRY; ARTICLE; BODY MASS; CHILD; CHROMOSOME MARKER; CONGENITAL MALFORMATION; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; HUMAN; INFANT; KARYOTYPE 45,X; KIDNEY MALFORMATION; MAJOR CLINICAL STUDY; PHENOTYPE; PRIORITY JOURNAL; PROSPECTIVE STUDY; SKELETON MALFORMATION; SOCIAL PSYCHOLOGY; TURNER SYNDROME; X CHROMOSOME; Y CHROMOSOME;

EID: 33947498699     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2006-0158     Document Type: Article

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