SCOPUS 정보 검색 플랫폼

Volumn 160, Issue 9, 2001, Pages 561-565

Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature

(9) Müsebeck, Jörg a Mohnike, Klaus a Beye, Petra a Tönnies, Holger b Neitzel, Heidemarie b Schnabel, Dirk c Grüters, Anette c Wieacker, Peter F a Stumm, Markus a

a OTTO VON GUERICKE UNIVERSITY (Germany)

b HUMBOLDT UNIVERSITY (Germany)

c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN (Germany)

Author keywords

FISH analysis; Forearm anomalies; Short stature; SHOX deletion

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOMAL LOCALIZATION; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; CONTROLLED STUDY; DYSCHONDROSTEOSIS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE FREQUENCY; HOMEOBOX; HUMAN; INFANT; MALE; METAPHASE; PRIORITY JOURNAL; SHORT STATURE; SKELETON MALFORMATION; X CHROMOSOME; Y CHROMOSOME;

ADOLESCENT; BODY HEIGHT; CHILD; CHILD, PRESCHOOL; FEMALE; GENE DELETION; GENES, HOMEOBOX; GENETIC SCREENING; GERMANY; HOMEODOMAIN PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; MALE; PHENOTYPE;

EID: 0035726095 PISSN: 03406199 EISSN: None Source Type: Journal
DOI: 10.1007/s004310100790 Document Type: Article

Times cited : (27)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.