Familial association of camptodactyly, mental retardation, whistling face and Pierre Robin sequence

Clinical Dysmorphology

Volumn 8, Issue 4, 1999, Pages 247-251

  Stoll, C ^a   Benoit, F ^c   Peter, M O ^c   Gasser, B ^b  

^a HÔPITAL DE HAUTEPIERRE   (France)

^b Hopital Central Strasbourg   (France)

^c NONE

Author keywords

Arthrogryposis; Freeman Sheldon syndrome; Mental retardation; Pierre Robin sequence

Indexed keywords

ARTICLE; CAMPTODACTYLY; CASE REPORT; CHILD; FACE DYSMORPHIA; FEMALE; FETUS ECHOGRAPHY; GROWTH RETARDATION; HOLOPROSENCEPHALY; HUMAN; HYDROCEPHALUS; HYPOKINESIA; MENTAL DEFICIENCY; NUCLEAR MAGNETIC RESONANCE IMAGING; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL; SIBLING; TRACHEOTOMY;

EID: 0032722613     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199910000-00003     Document Type: Article

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