SCOPUS 정보 검색 플랫폼

Volumn 51, Issue 1-2, 2001, Pages 114-116

Identification of mtDNA mutation in a Pedigree with gestational diabetes, deafness, Wolff-Parkinson-White syndrome and placenta accreta

(6) Aggarwal, P a Gill Randall, R a Wheatley, T b Buchalter, M B c Metcalfe, J b Alcolado, J C a

a CARDIFF UNIVERSITY (United Kingdom)

b PRINCESS ROYAL HOSPITAL (United Kingdom)

c UNIVERSITY HOSPITAL OF WALES (United Kingdom)

Author keywords

Diabetes; Mitochondrial DNA; Wolff Parkinson White syndrome

Indexed keywords

ADENINE; GUANINE; MITOCHONDRIAL DNA;

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE MARKER; EXTRACHROMOSOMAL INHERITANCE; FAMILY HISTORY; FEMALE; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; MALE; MELAS SYNDROME; NUCLEIC ACID BASE SUBSTITUTION; PEDIGREE ANALYSIS; PHENOTYPE; PLACENTA ACCRETA; PREGNANCY DIABETES MELLITUS; WOLFF PARKINSON WHITE SYNDROME;

ADULT; DEAFNESS; DIABETES, GESTATIONAL; DNA, MITOCHONDRIAL; FEMALE; HUMANS; PEDIGREE; PLACENTA ACCRETA; POINT MUTATION; POLYMERASE CHAIN REACTION; PREGNANCY; WOLFF-PARKINSON-WHITE SYNDROME;

EID: 0035205506 PISSN: 00015652 EISSN: None Source Type: Journal
DOI: 10.1159/000022950 Document Type: Article

Times cited : (23)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.