SCOPUS 정보 검색 플랫폼

Volumn 108, Issue 6, 2001, Pages 511-515

Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation

(9) Rio, Marlène a Ozilou, Catherine a Cormier Daire, Valérie a Turleau, Catherine a Prieur, Marguerite a Vekemans, Michel a Chauveau, Pierre b Munnich, Arnold a Colleaux, Laurence a

a HÔPITAL NECKER ENFANTS MALADES (France)

b Centre Infantile Raymond Lerch (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BEHAVIOR DISORDER; CASE REPORT; CHROMOSOMAL LOCALIZATION; CHROMOSOME 17Q; CHROMOSOME MARKER; CHROMOSOME REARRANGEMENT; DISEASE SEVERITY; FACE DYSMORPHIA; FLUORESCENCE ANALYSIS; GENETIC ANALYSIS; GENOME IMPRINTING; GENOTYPE; HETEROZYGOTE DETECTION; HUMAN; HYPERACTIVITY; HYPERTELORISM; MALE; MATERNAL DISEASE; MATERNAL HETERODISOMY; MENTAL DEFICIENCY; MOTOR DYSFUNCTION; NUMERICAL CHROMOSOME ABERRATION; PRESCHOOL CHILD; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TELOMERE; TRISOMY;

CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 17; CYTOGENETIC ANALYSIS; DNA; FAMILY HEALTH; FEMALE; GENOMIC IMPRINTING; GENOTYPE; HUMANS; KARYOTYPING; MALE; MENTAL RETARDATION; MICROSATELLITE REPEATS;

EID: 0034893354 PISSN: 03406717 EISSN: None Source Type: Journal
DOI: 10.1007/s004390100522 Document Type: Article

Times cited : (10)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.