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Volumn 107, Issue 1, 2002, Pages 38-42

Craniosynostosis, ectopia lentis, and congenital heart defects: Further delineation of an autosomal dominant syndrome with incomplete penetrance

(2) Quercia, N L a Teebi, A S a

a HOSPITAL FOR SICK CHILDREN (Canada)

Author keywords

Craniosynostosis; Ectopia lentis; Peripheral pulmonic branch stenosis

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; CRANIOFACIAL SYNOSTOSIS; DISEASE COURSE; ECTOPIA LENTIS; FEMALE; FOLLOW UP; HEART ATRIUM SEPTUM DEFECT; HUMAN; INTELLIGENCE; MITRAL VALVE PROLAPSE; MYOPIA; PENETRANCE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CRANIOSYNOSTOSES; ECTOPIA LENTIS; FEMALE; GENES, DOMINANT; HEART DEFECTS, CONGENITAL; HUMANS; MALE; PEDIGREE; PENETRANCE; SYNDROME;

EID: 0036134786 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10124 Document Type: Article

Times cited : (3)

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