SCOPUS 정보 검색 플랫폼

Volumn 91, Issue 6, 1993, Pages 589-598

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization

(6) Plattner, Rina a Heerema, Nyla A a Howard Peebles, Patricia N b,c Miles, Judith H d Soukup, Shirley e Palmer, Catherine G a

a INDIANA UNIVERSITY SCHOOL OF MEDICINE (United States)

b GENETICS AND IVF INSTITUTE (United States)

c VIRGINIA COMMONWEALTH UNIVERSITY (United States)

d UNIVERSITY OF MISSOURI (United States)

e UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SATELLITE DNA;

ADULT; ARTICLE; CHILD; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CLINICAL FEATURE; DNA PROBE; FEMALE; FETUS; FLUORESCENCE; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; MALE; MARKER CHROMOSOME; NEWBORN; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ABNORMALITIES; ADULT; CASE REPORT; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; DNA PROBES; DNA, SATELLITE; FEMALE; GENETIC MARKERS; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; PREGNANCY; PRENATAL DIAGNOSIS; RING CHROMOSOMES; RISK; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027184219 PISSN: 03406717 EISSN: 14321203 Source Type: Journal
DOI: 10.1007/BF00205086 Document Type: Article

Times cited : (73)

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