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P-E Mullis

Showing results (71-80 of 78) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|May 14, 1999
"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiencyJ Deladoëy, C Flück, A Büyükgebiz, et al.
Mineral and Electrolyte Metabolism|January 1, 1997
Extracellular magnesium depletion in pediatric patients with insulin-dependent diabetes mellitusM J Husmann, P Fuchs, A C Truttmann, et al.
Diabetologia|April 25, 2001
Epidemiology of type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decadeE J Schoenle, M Lang-Muritano, S Gschwend, et al.
Clinical Nephrology|March 26, 2003
Which factors account for renal stone formation in cystic fibrosis?R von der Heiden, A P G Balestra, M G Bianchetti, et al.
Nature Genetics|December 17, 1997
Positional cloning of the APECED geneK Nagamine, P Peterson, H S Scott, et al.
Nature Genetics|February 14, 1998
Mutations in PROP1 cause familial combined pituitary hormone deficiencyW Wu, J D Cogan, R W Pfäffle, et al.
The Journal of Clinical Endocrinology and Metabolism|May 3, 2012
Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individualsN Camats, A V Pandey, M Fernández-Cancio, et al.
American Journal of Human Genetics|October 1, 1996
Genetic homogeneity of autoimmune polyglandular disease type IP Björses, J Aaltonen, A Vikman, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
The Journal of Clinical Endocrinology and Metabolism|May 14, 1999
"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiencyJ Deladoëy, C Flück, A Büyükgebiz, et al.
Mineral and Electrolyte Metabolism|January 1, 1997
Extracellular magnesium depletion in pediatric patients with insulin-dependent diabetes mellitusM J Husmann, P Fuchs, A C Truttmann, et al.
Diabetologia|April 25, 2001
Epidemiology of type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decadeE J Schoenle, M Lang-Muritano, S Gschwend, et al.
Clinical Nephrology|March 26, 2003
Which factors account for renal stone formation in cystic fibrosis?R von der Heiden, A P G Balestra, M G Bianchetti, et al.
Nature Genetics|December 17, 1997
Positional cloning of the APECED geneK Nagamine, P Peterson, H S Scott, et al.
Nature Genetics|February 14, 1998
Mutations in PROP1 cause familial combined pituitary hormone deficiencyW Wu, J D Cogan, R W Pfäffle, et al.
The Journal of Clinical Endocrinology and Metabolism|May 3, 2012
Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individualsN Camats, A V Pandey, M Fernández-Cancio, et al.
American Journal of Human Genetics|October 1, 1996
Genetic homogeneity of autoimmune polyglandular disease type IP Björses, J Aaltonen, A Vikman, et al.
Pageof 8