Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients

American Journal of Medical Genetics

Volumn 102, Issue 1, 2001, Pages 11-17

  Wang, Lisa L ^a   Levy, Moise L ^a   Lewis, Richard A ^a   Chintagumpala, Murali M ^a   Lev, Dorit ^b   Rogers, Maureen ^c   Plon, Sharon E ^a,d  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b WOLFSON MEDICAL CENTER   (Israel)

^c CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^d FACMG   (United States)

Author keywords

Cancer; Cataract; Chromosomal instability; Genetics; Osteosarcoma; Poikiloderma; Radial ray defect; Rash

Indexed keywords

ANTINEOPLASTIC AGENT; GROWTH HORMONE;

ADOLESCENT; ADULT; ARTICLE; CATARACT; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COHORT ANALYSIS; CYTOGENETICS; FEMALE; GASTROINTESTINAL DISEASE; GENETIC HETEROGENEITY; GENODERMATOSIS; HUMAN; INFANT; MALE; OSTEOSARCOMA; PREVALENCE; PRIORITY JOURNAL; ROTHMUND THOMSON SYNDROME; SHORT STATURE; SKELETON MALFORMATION;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 7; CHROMOSOMES, HUMAN, PAIR 8; COHORT STUDIES; CYTOGENETIC ANALYSIS; FEMALE; HUMANS; INFANT; KARYOTYPING; MALE; ROTHMUND-THOMSON SYNDROME; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0035934019     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010722)102:1<11::AID-AJMG1413>3.0.CO;2-A     Document Type: Article

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