SCOPUS 정보 검색 플랫폼

Volumn 30, Issue 6, 2007, Pages 1613-1614

Digenic inheritance of hepatocyte nuclear factor-1α and -1β with maturity-onset diabetes of the young, polycystic thyroid, and urogenital malformations

(9) Karges, Beate a Bergmann, Carsten b Scholl, Katrina a Heinze, Eberhard a Rasche, Franz Maximilian c Zerres, Klaus b Debatin, Klaus Michael a Wabitsch, Martin a Karges, Wolfram b

a UNIVERSITY HOSPITAL ULM (Germany)

b RWTH AACHEN UNIVERSITY (Germany)

c UNIVERSITY OF ULM (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

C PEPTIDE; CREATININE; GLIMEPIRIDE; GLUCOSE; GLUTAMATE DECARBOXYLASE 65 ANTIBODY; HEMOGLOBIN A1C; HEPATOCYTE NUCLEAR FACTOR 1ALPHA; HEPATOCYTE NUCLEAR FACTOR 1BETA; INSULIN; THYROTROPIN;

ABDOMEN; ABDOMINAL DISCOMFORT; ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME; ECHOGRAPHY; FAMILY HISTORY; FEMALE; GLUCOSE BLOOD LEVEL; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HYPOPLASIA; INSULIN RELEASE; KIDNEY AGENESIS; KIDNEY FUNCTION; LIVER FUNCTION; MATURITY ONSET DIABETES MELLITUS; MISSENSE MUTATION; POLYCYSTIC THYROID; SINGLE NUCLEOTIDE POLYMORPHISM; THYROID DISEASE; THYROID FUNCTION; UROGENITAL TRACT MALFORMATION; UTERINE CERVIX DISEASE; UTERINE CERVIX HEMIATRESIA; UTERUS DIDELPHYS; UTERUS HORN;

ADOLESCENT; DIABETES MELLITUS, TYPE 2; FEMALE; HEPATOCYTE NUCLEAR FACTOR 1; HEPATOCYTE NUCLEAR FACTOR 1-BETA; HETEROZYGOTE DETECTION; HUMANS; INSULIN; INSULIN-SECRETING CELLS; MALE; MUTATION; PEDIGREE; SEQUENCE DELETION; THYROID DISEASES; UROGENITAL ABNORMALITIES;

EID: 34249889040 PISSN: 01495992 EISSN: 01495992 Source Type: Journal
DOI: 10.2337/dc06-2618 Document Type: Article

Times cited : (16)

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