SCOPUS 정보 검색 플랫폼

Neurology

Volumn 54, Issue 8, 2000, Pages 1701-1703

Septo-optic dysplasia plus: A spectrum of malformations of cortical development

(5) Miller, S P b Shevell, M I a Patenaude, Y a Poulin, C b O'Gorman, A M a

a MONTREAL CHILDREN S HOSPITAL (Canada)

b Montreal Children's Hospital ^*

Author keywords

Cortical development; Septooptic dysplasia plus

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CASE REPORT; CHILD; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DYSPLASIA; FEMALE; HUMAN; MALE; MOTOR DYSFUNCTION; OPTIC NERVE; PRIORITY JOURNAL; SCHIZENCEPHALY; SEPTUM PELLUCIDUM; SYNDROME DELINEATION;

EID: 0034102036 PISSN: 00283878 EISSN: None Source Type: Journal
DOI: 10.1212/WNL.54.8.1701 Document Type: Article

Times cited : (113)

References (10)

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5
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7
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- Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.