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Willy Lissens

Showing results (1-10 of 68) with videos related to

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Biochimica Et Biophysica Acta|May 29, 2012
X chromosomal mutations and spermatogenic failureKatrien Stouffs, Willy Lissens
Prenatal Diagnosis|January 22, 2005
A novel L1CAM mutation with L1 spectrum disordersFatma Silan, Ismail Ozdemir, Willy Lissens
Annales D'Endocrinologie|April 29, 2014
Genetic causes of male infertilityKatrien Stouffs, Sara Seneca, Willy Lissens
Human Reproduction Update|October 21, 2010
What about gr/gr deletions and male infertility? Systematic review and meta-analysisKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
Thrombosis Research|April 4, 2015
Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophiliaChristelle Orlando, Olivier Heylen, Willy Lissens, et al.
Asian Journal of Andrology|December 6, 2011
Genetic causes of spermatogenic failureAnnelien Massart, Willy Lissens, Herman Tournaye, et al.
Human Reproduction Update|June 12, 2009
Male infertility and the involvement of the X chromosomeKatrien Stouffs, Herman Tournaye, Inge Liebaers, et al.
European Journal of Internal Medicine|April 24, 2007
A case of thyroid hormone resistance: Prospective follow-up during pregnancy and obstetric outcomeDany Massaad, Kris Poppe, Willy Lissens, et al.
Thrombosis and Haemostasis|November 26, 2011
Identification of two de novo mutations responsible for type I antithrombin deficiencyChristelle Orlando, Willy Lissens, Daniele Hasaerts, et al.
Human Mutation|February 20, 2013
Systematic detection of pathogenic alu element insertions in NGS-based diagnostic screens: the BRCA1/BRCA2 exampleSylvia De Brakeleer, Jacques De Grève, Willy Lissens, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Biochimica Et Biophysica Acta|May 29, 2012
X chromosomal mutations and spermatogenic failureKatrien Stouffs, Willy Lissens
Prenatal Diagnosis|January 22, 2005
A novel L1CAM mutation with L1 spectrum disordersFatma Silan, Ismail Ozdemir, Willy Lissens
Annales D'Endocrinologie|April 29, 2014
Genetic causes of male infertilityKatrien Stouffs, Sara Seneca, Willy Lissens
Human Reproduction Update|October 21, 2010
What about gr/gr deletions and male infertility? Systematic review and meta-analysisKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
Thrombosis Research|April 4, 2015
Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophiliaChristelle Orlando, Olivier Heylen, Willy Lissens, et al.
Asian Journal of Andrology|December 6, 2011
Genetic causes of spermatogenic failureAnnelien Massart, Willy Lissens, Herman Tournaye, et al.
Human Reproduction Update|June 12, 2009
Male infertility and the involvement of the X chromosomeKatrien Stouffs, Herman Tournaye, Inge Liebaers, et al.
European Journal of Internal Medicine|April 24, 2007
A case of thyroid hormone resistance: Prospective follow-up during pregnancy and obstetric outcomeDany Massaad, Kris Poppe, Willy Lissens, et al.
Thrombosis and Haemostasis|November 26, 2011
Identification of two de novo mutations responsible for type I antithrombin deficiencyChristelle Orlando, Willy Lissens, Daniele Hasaerts, et al.
Human Mutation|February 20, 2013
Systematic detection of pathogenic alu element insertions in NGS-based diagnostic screens: the BRCA1/BRCA2 exampleSylvia De Brakeleer, Jacques De Grève, Willy Lissens, et al.
Pageof 7