Citation: O. Hiort et al., PHYSIOLOGY AND PATHOPHYSIOLOGY OF ANDROGEN ACTION, Bailliere's clinical endocrinology and metabolism, 12(1), 1998, pp. 115-132
Authors:
AUMULLER G
HOLTERHUS PM
KONRAD L
VONRAHDEN B
HIORT O
ESQUENET M
VERHOEVEN G
Citation: G. Aumuller et al., IMMUNOHISTOCHEMISTRY AND IN-SITU HYBRIDIZATION OF THE ANDROGEN RECEPTOR IN THE DEVELOPING HUMAN PROSTATE, Anatomy and embryology, 197(3), 1998, pp. 199-208
Citation: O. Hiort, FROM GENOTYPE TO PHENOTYPE - MOLECULAR-GE NETIC ANALYSIS IN INTERSEX DISORDERS, Monatsschrift fur Kinderheilkunde, 146(2), 1998, pp. 86-91
Authors:
HIORT O
SINNECKER GHG
HOLTERHUS PM
NITSCHE EM
KRUSE K
Citation: O. Hiort et al., INHERITED AND DE-NOVO ANDROGEN RECEPTOR GENE-MUTATIONS - INVESTIGATION OF SINGLE-CASE FAMILIES, The Journal of pediatrics, 132(6), 1998, pp. 939-943
Authors:
SINNECKER GHG
HIORT O
NITSCHE EM
HOLTERHUS PM
KRUSE K
Citation: Ghg. Sinnecker et al., FUNCTIONAL ASSESSMENT AND CLINICAL CLASSIFICATION OF ANDROGEN SENSITIVITY IN PATIENTS WITH MUTATIONS OF THE ANDROGEN RECEPTOR GENE, European journal of pediatrics, 156(1), 1997, pp. 7-14
Authors:
HOLTERHUS PM
BRUGGENWIRTH HT
HIORT O
KLEINKAUFHOUCKEN A
KRUSE K
SINNECKER GHG
BRINKMANN AO
Citation: Pm. Holterhus et al., MOSAICISM DUE TO A SOMATIC MUTATION OF THE ANDROGEN RECEPTOR GENE DETERMINES PHENOTYPE IN ANDROGEN INSENSITIVITY SYNDROME, The Journal of clinical endocrinology and metabolism, 82(11), 1997, pp. 3584-3589
Authors:
HIORT O
WILLENBRING H
ALBERS N
HECKER W
ENGERT J
DIBBELT L
SINNECKER GHG
Citation: O. Hiort et al., MOLECULAR-GENETIC ANALYSIS AND HUMAN CHORIONIC-GONADOTROPIN STIMULATION TESTS IN THE DIAGNOSIS OF PREPUBERTAL PATIENTS WITH PARTIAL 5-ALPHA-REDUCTASE DEFICIENCY, European journal of pediatrics, 155(6), 1996, pp. 445-451
Authors:
HIORT O
SINNECKER GHG
HOLTERHUS PM
NITSCHE EM
KRUSE K
Citation: O. Hiort et al., THE CLINICAL AND MOLECULAR-SPECTRUM OF ANDROGEN INSENSITIVITY SYNDROMES, American journal of medical genetics, 63(1), 1996, pp. 218-222
Authors:
SINNECKER GHG
HIORT O
DIBBELT L
ALBERS N
DORR HG
HAUSS H
HEINRICH U
HEMMINGHAUS M
HOEPFFNER W
HOLDER M
SCHNABEL D
KRUSE K
Citation: Ghg. Sinnecker et al., PHENOTYPIC CLASSIFICATION OF MALE PSEUDOHERMAPHRODITISM DUE TO STEROID 5-ALPHA-REDUCTASE-2 DEFICIENCY, American journal of medical genetics, 63(1), 1996, pp. 223-230
Authors:
HIORT O
NABER SP
LEHNERS A
MULETTAFEURER S
SINNECKER GHG
ZOLLNER A
KOMMINOTH P
Citation: O. Hiort et al., THE ROLE OF ANDROGEN RECEPTOR GENE-MUTATIONS IN MALE BREAST-CARCINOMA, The Journal of clinical endocrinology and metabolism, 81(9), 1996, pp. 3404-3407
Authors:
HIORT O
SINNECKER GHG
WILLENBRING H
LEHNERS A
ZOLLNER A
STRUVE D
Citation: O. Hiort et al., NONISOTOPIC SINGLE-STRAND CONFORMATION ANALYSIS OF THE 5-ALPHA-REDUCTASE TYPE-2 GENE FOR THE DIAGNOSIS OF 5-ALPHA-REDUCTASE DEFICIENCY, The Journal of clinical endocrinology and metabolism, 81(9), 1996, pp. 3415-3418
Authors:
HOCHBERG Z
CHAYEN R
REISS N
FALIK Z
MAKLER A
MUNICHOR M
FARKAS A
GOLDFARB H
OHANA N
HIORT O
Citation: Z. Hochberg et al., CLINICAL, BIOCHEMICAL, AND GENETIC FINDINGS IN A LARGE PEDIGREE OF MALE AND FEMALE-PATIENTS WITH 5-ALPHA-REDUCTASE-2 DEFICIENCY, The Journal of clinical endocrinology and metabolism, 81(8), 1996, pp. 2821-2827
Authors:
KOMMINOTH P
MULETTAFEURER S
SAREMASLANI P
KUNZ EK
MATIASGUIU X
HIORT O
SCHRODER S
SEELENTAG WKF
ROTH J
HEITZ PU
Citation: P. Komminoth et al., MOLECULAR DIAGNOSIS OF MULTIPLE ENDOCRINE NEOPLASIA (MEN) IN PARAFFIN-EMBEDDED SPECIMENS, Endocrine pathology, 6(4), 1995, pp. 267-278
Citation: O. Hiort et Gt. Klauber, TRUE HERMAPHRODITISM WITH 46,XY KARYOTYPE AND A POINT MUTATION IN THESRY GENE, The Journal of pediatrics, 126(6), 1995, pp. 1022-1022
Authors:
KOMMINOTH P
KUNZ EK
MATIASGUIU X
HIORT O
CHRISTENSEN G
COLOMER A
ROTH J
HEITZ PU
Citation: P. Komminoth et al., ANALYSIS OF RET PROTOONCOGENE POINT MUTATIONS DISTINGUISHES HERITABLEFROM NONHERITABLE MEDULLARY-THYROID CARCINOMAS, Cancer, 76(3), 1995, pp. 479-489
Authors:
HIORT O
WODTKE A
STRUVE D
ZOLLNER A
SINNECKER GHG
ALBERS N
BEYE M
BEYER P
BIRR C
BLUNCK W
BRACK C
BRAMSWIG J
DORR HG
GAL A
HECKER W
HEIDEMANN P
HEINRICH U
HEISE HR
HESSE V
HINKEL M
HOEPFFNER W
HOLDER M
KEIM L
KLASEN M
KORSCH E
KRUGER G
LANDENDORFER W
MIX M
MORLOT M
MUHLENBERG R
OTTEN A
PARTSCH CJ
PELZ L
VONPETRYKOWSKI W
RABL W
REICH H
SCHENK B
SCHNABEL D
SIPPELL W
Citation: O. Hiort et al., DETECTION OF POINT MUTATIONS IN THE ANDROGEN RECEPTOR GENE USING NONISOTOPIC SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS, Human molecular genetics, 3(7), 1994, pp. 1163-1166
Authors:
HIORT O
KLAUBER G
CENDRON M
SINNECKER GHG
KEIM L
SCHWINGER E
WOLFE HJ
YANDELL DW
Citation: O. Hiort et al., MOLECULAR CHARACTERIZATION OF THE ANDROGEN RECEPTOR GENE IN BOYS WITHHYPOSPADIAS, European journal of pediatrics, 153(5), 1994, pp. 317-321
Authors:
KOMMINOTH P
KUNZ E
HIORT O
SCHRODER S
MATIASGUIU X
CHRISTIANSEN G
ROTH J
HEITZ PU
Citation: P. Komminoth et al., DETECTION OF RET PROTOONCOGENE POINT MUTATIONS IN PARAFFIN-EMBEDDED PHEOCHROMOCYTOMA SPECIMENS BY NONRADIOACTIVE SINGLE-STRAND CONFORMATIONPOLYMORPHISM ANALYSIS AND DIRECT SEQUENCING, The American journal of pathology, 145(4), 1994, pp. 922-929
Authors:
HIORT O
HUANG Q
SINNECKER GHG
SADEGHINEJAD A
KRUSE K
WOLFE HJ
YANDELL DW
Citation: O. Hiort et al., SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS OF ANDROGEN RECEPTORGENE-MUTATIONS IN PATIENTS WITH ANDROGEN INSENSITIVITY SYNDROMES - APPLICATION FOR DIAGNOSIS, GENETIC-COUNSELING, AND THERAPY, The Journal of clinical endocrinology and metabolism, 77(1), 1993, pp. 262-266