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J Glatzl

Showing results (21-30 of 27) with videos related to

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The Journal of Urology|September 25, 1997
Androgen receptor point mutations as the underlying molecular defect in 2 patients with androgen insensitivity syndromeC Radmayr, Z Culig, J Glatzl, et al.
Clinical Nephrology|March 1, 1993
Hereditary complete deficiency of the fourth component of complement: effects on the kidneyK Lhotta, W Thoenes, J Glatzl, et al.
European Journal of Pediatrics|January 1, 1993
Precocious puberty due to a lipid-cell tumour of the ovaryK Dengg, F M Fink, A Heitger, et al.
Padiatrie Und Padologie|January 1, 1980
Hereditary deficiency of adenine phosphoribosyl transferaseF Schabel, W Doppler, M Hirsch-Kauffmann, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 1, 1993
Characterization of two point mutations in the androgen receptor gene of patients with perineoscrotal hypospadiaF Kaspar, A C Cato, A Denninger, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1996
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyS Geley, K Kapelari, K Jöhrer, et al.
Klinische Padiatrie|March 6, 1999
Screening of patients with Turner syndrome for "hidden" Y-mosaicismI Vlasak, E Plöchl, G Kronberger, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
The Journal of Urology|September 25, 1997
Androgen receptor point mutations as the underlying molecular defect in 2 patients with androgen insensitivity syndromeC Radmayr, Z Culig, J Glatzl, et al.
Clinical Nephrology|March 1, 1993
Hereditary complete deficiency of the fourth component of complement: effects on the kidneyK Lhotta, W Thoenes, J Glatzl, et al.
European Journal of Pediatrics|January 1, 1993
Precocious puberty due to a lipid-cell tumour of the ovaryK Dengg, F M Fink, A Heitger, et al.
Padiatrie Und Padologie|January 1, 1980
Hereditary deficiency of adenine phosphoribosyl transferaseF Schabel, W Doppler, M Hirsch-Kauffmann, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 1, 1993
Characterization of two point mutations in the androgen receptor gene of patients with perineoscrotal hypospadiaF Kaspar, A C Cato, A Denninger, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1996
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyS Geley, K Kapelari, K Jöhrer, et al.
Klinische Padiatrie|March 6, 1999
Screening of patients with Turner syndrome for "hidden" Y-mosaicismI Vlasak, E Plöchl, G Kronberger, et al.
Pageof 3