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Volumn 143, Issue 12, 2007, Pages 1282-1286

A newly recognized craniosynostosis syndrome with features of Aarskog-Scott and Teebi syndromes

Author keywords

Craniosynostosis; Faciogenital dysplasia; Short stature; Teebi hypertelorism syndrome (brachycephalofrontal dysplasia)

Indexed keywords

ADOLESCENT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; CRANIOFACIAL SYNOSTOSIS; FACIOGENITAL DYSPLASIA; HUMAN; HYPERTELORISM; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; SYNDROME DELINEATION; TEEBI SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 34249875141     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31780     Document Type: Article
Times cited : (4)

References (10)
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  • 3
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  • 4
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    • Orrico A, Galli L, Buoni S, Hayek G, Luchetti A, Lorenzini S, Zappella M, Pomponi MG, Sorrentino V. 2005. Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q). Am J Med Genet Part A 135A:99-102.
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  • 8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.