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Clinical Dysmorphology

Volumn 11, Issue 2, 2002, Pages 113-115

Microdeletion 22q11.2, Kousseff syndrome and spina bifida

(4) Seller, Mary J a,b Mohammed, Shehla b Russell, Jo c Ogilvie, Caroline c

a KING'S COLLEGE LONDON (United Kingdom)

b GUY S HOSPITAL (United Kingdom)

c Guy's Tower ^* (United Kingdom)

Author keywords

Deletion 22q11.2; DiGeorge syndrome; Kousseff syndrome; Neural tube defects; Spina bifida; Velocardiofacial syndrome

Indexed keywords

ARTICLE; AUTOPSY; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; CLEFT PALATE; CYTOGENETICS; DIGEORGE SYNDROME; FACE DYSMORPHIA; FEMALE; FETUS; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; HEART VENTRICLE SEPTUM DEFECT; HUMAN; KOUSSEFF SYNDROME; NEURAL TUBE DEFECT; PREGNANCY TERMINATION; PRIORITY JOURNAL; SPINA BIFIDA; VELOCARDIOFACIAL SYNDROME; ADOLESCENT; CHROMOSOME 22; FACIES; GENE DELETION; GENETICS; MENINGOCELE; MULTIPLE MALFORMATION SYNDROME; PREGNANCY; SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHROMOSOMES, HUMAN, PAIR 22; FACIES; FEMALE; HUMANS; MENINGOCELE; PREGNANCY; SEQUENCE DELETION; SPINAL DYSRAPHISM; SYNDROME;

EID: 0036009946 PISSN: 09628827 EISSN: None Source Type: Journal
DOI: 10.1097/00019605-200204000-00007 Document Type: Article

Times cited : (14)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.