SCOPUS 정보 검색 플랫폼

Volumn 38, Issue 12, 2001, Pages 882-884

High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample [10]

(6) Ehrlich, M a Tsien, F a Herrera, D a Blackman, V a Roggenbuck, J a Tuck Muller, C M a

a TULANE UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA METHYLTRANSFERASE;

ADULT; AMNIOTIC FLUID CELL; CASE REPORT; CHORION VILLUS; CHORION VILLUS SAMPLING; CHROMOSOME 1; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; DNA SEQUENCE; FACE MALFORMATION; FEMALE; FETUS; GENE MUTATION; HETEROCHROMATIN; HUMAN; HUMAN TISSUE; ICF SYNDROME; IMMUNE DEFICIENCY; LETTER; PRIORITY JOURNAL;

ADULT; CELLS, CULTURED; CENTROMERE; CHORIONIC VILLI; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 16; CRANIOFACIAL ABNORMALITIES; DNA (CYTOSINE-5-)-METHYLTRANSFERASE; DNA METHYLATION; FEMALE; GENE FREQUENCY; GENETIC COUNSELING; GENETIC SCREENING; HETEROCHROMATIN; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT; INFANT, NEWBORN; MALE; PREGNANCY; PRENATAL DIAGNOSIS; SYNDROME; TRISOMY;

EID: 0035662541 PISSN: 00222593 EISSN: None Source Type: Journal
DOI: None Document Type: Letter

Times cited : (9)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.