Confirmation of the autosomal recessive syndrome of ectopia lentis and distinctive craniofacial appearance

American Journal of Medical Genetics

Volumn 99, Issue 3, 2001, Pages 185-189

  Haddad, Randa ^a   Uwaydat, Sami ^a   Dakroub, Rola ^a   Traboulsi, Elias I ^b  

^a AMERICAN UNIVERSITY OF BEIRUT   (Lebanon)

^b LERNER RESEARCH INSTITUTE   (United States)

Author keywords

Autosomal recessive; Craniofacial dysmorphism; Dislocated lens; Druze; Glaucoma; Lebanon; Syndrome

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CLINICAL FEATURE; CONNECTIVE TISSUE DISEASE; ECTOPIA LENTIS; FACE DYSMORPHIA; FAMILY STUDY; FEMALE; GENE MUTATION; GLAUCOMA; HUMAN; LEBANON; LENS DISEASE; MARFAN SYNDROME; PRIORITY JOURNAL;

ECTOPIA LENTIS; FACIES; FEMALE; GENES, RECESSIVE; HUMANS; MALE; PEDIGREE; SYNDROME;

EID: 0035869199     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1156>3.0.CO;2-V     Document Type: Article

References (9)

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9. The metacarpal index in Jamaican children and adults