SCOPUS 정보 검색 플랫폼

Volumn 38, Issue 12, 2001, Pages 850-852

Trinucleotide repeat contraction: A pitfall in prenatal diagnosis of myotonic dystrophy [2]

(9) Amiel, J a Raclin, V a Jouannic, J M a Morichon, N a Hoffman Radvanyi, H a Dommergues, M a Feingold, J a Munnich, A a Bonnefont, J P a

a HÔPITAL NECKER ENFANTS MALADES (France)

Author keywords

[No Author keywords available]

Indexed keywords

3' UNTRANSLATED REGION; ADULT; ALLELE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; FEMALE; FETUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; HUMAN CELL; LETTER; MYOTONIC DYSTROPHY; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT; VERTICAL TRANSMISSION;

ADULT; ALLELES; BLOTTING, SOUTHERN; DNA MUTATIONAL ANALYSIS; FEMALE; FETUS; HUMANS; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MUTAGENESIS; MYOTONIC DYSTROPHY; PEDIGREE; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS; PROTEIN-SERINE-THREONINE KINASES; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 0035659065 PISSN: 00222593 EISSN: None Source Type: Journal
DOI: None Document Type: Letter

Times cited : (5)

References (14)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.