Associated malformations in patients with limb reduction deficiencies

European Journal of Medical Genetics

Volumn 53, Issue 5, 2010, Pages 286-290

  Stoll, Claude ^a   Alembik, Yves ^a   Dott, Beatrice ^a   Roth, Marie Paule ^a  

^a UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

Congenital malformations; Limb malformations; Limb reduction deficiencies

Indexed keywords

AMNION BAND SYNDROME; ANGIOOSTEOHYPERTROPHY SYNDROME; ARTICLE; CENTRAL NERVOUS SYSTEM MALFORMATION; CHROMOSOME ABERRATION; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; CONTROLLED STUDY; DE LANGE SYNDROME; DIGESTIVE SYSTEM; DISEASE ASSOCIATION; DISEASE SURVEILLANCE; DYSOSTOSIS; EEC SYNDROME; FANCONI ANEMIA; GENETICS; GENITAL MALFORMATION; GOLDENHAR SYNDROME; HOLT ORAM SYNDROME; HUMAN; INFANT; LIMB REDUCTION DEFECT; LIVE BIRTH; MAJOR CLINICAL STUDY; MOEBIUS SYNDROME; POLAND SYNDROME; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PREVALENCE; RADIUS APLASIA; RENAL SYSTEM PARAMETERS; ROBERTS SYNDROME; RUBINSTEIN SYNDROME; SCREENING; SMITH LEMLI OPITZ SYNDROME; STILLBIRTH; THROMBOCYTOPENIA; TOWNES BROCKS SYNDROME; TRISOMY;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; LIMB DEFORMITIES, CONGENITAL; POLAND; PREGNANCY; PRENATAL DIAGNOSIS; PREVALENCE; STILLBIRTH; SYNDROME;

EID: 77956901183     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2010.07.012     Document Type: Article

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