Familial occurrence of ptosis, nasal speech, prominent ears, hand anomalies and learning problems

European Journal of Medical Genetics

Volumn 53, Issue 4, 2010, Pages 192-196

  Belligni, Elga F ^a,b   Hennekam, Raoul C M ^b,c,d  

^a UNIVERSITY OF TURIN   (Italy)

^b GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

Autosomal dominant; Cleft palate; Hand anomaly; Mental retardation; Ptosis; Velum insufficiency

Indexed keywords

ADULT; ARTICLE; ASTIGMATISM; BRACHYDACTYLY; CHEEK; CHILD; CLEFT PALATE; CLINICAL ARTICLE; CLINICAL FEATURE; EAR MALFORMATION; FAMILIAL INCIDENCE; FEMALE; HAND MALFORMATION; HUMAN; HYPOGLYCEMIA; INHERITANCE; LEARNING DISORDER; MALE; MOUTH; MYOPIA; NOSE SEPTUM; PERCEPTION DEAFNESS; PRESCHOOL CHILD; PTOSIS; SPEECH DISORDER; SYNDACTYLY; CASE REPORT; EAR; FAMILY; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; NEWBORN; PATHOLOGY; PEDIGREE; PROGNOSIS;

ADULT; BLEPHAROPTOSIS; CHILD; CHILD, PRESCHOOL; EAR; FAMILY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAND DEFORMITIES; HUMANS; INFANT, NEWBORN; LEARNING DISORDERS; MALE; MIDDLE AGED; PEDIGREE; PROGNOSIS; SPEECH DISORDERS;

EID: 77954387226     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2010.03.009     Document Type: Article

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