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Journal of Medical Genetics

Volumn 35, Issue 6, 1998, Pages 497-501

Meckel syndrome

(2) Salonen, Riitta a Paavola, Paulina b

a HELSINKI UNIVERSITY CENTRAL HOSPITAL (Finland)

b NATIONAL PUBLIC HEALTH INSTITUTE (Finland)

Author keywords

Meckel syndrome

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CENTRAL NERVOUS SYSTEM MALFORMATION; CHROMOSOME 17Q; CONNECTIVE TISSUE; DNA DETERMINATION; ENCEPHALOMENINGOCELE; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; HAPLOTYPE; HUMAN; KIDNEY CYST; LIVER FIBROSIS; MECKEL SYNDROME; POLYDACTYLY; PREGNANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ULTRASOUND;

EID: 0031799081 PISSN: 00222593 EISSN: None Source Type: Journal
DOI: 10.1136/jmg.35.6.497 Document Type: Article

Times cited : (97)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.