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Willy Lissens

Showing results (11-20 of 68) with videos related to

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Human Reproduction (Oxford, England)|March 26, 2005
The choice and outcome of the fertility treatment of 38 couples in whom the male partner has a Yq microdeletionKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
Journal of the Neurological Sciences|July 15, 2011
A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperatureVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
European Journal of Human Genetics : EJHG|November 25, 2004
Possible role of USP26 in patients with severely impaired spermatogenesisKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
International Journal of Andrology|November 24, 2006
Alterations of the USP26 gene in Caucasian menKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
Fertility and Sterility|October 11, 2005
SYCP3 mutations are uncommon in patients with azoospermiaKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
Fertility and Sterility|February 9, 2008
Is there a role for the nuclear export factor 2 gene in male infertility?Katrien Stouffs, Herman Tournaye, Josiane Van der Elst, et al.
JIMD Reports|February 23, 2013
Pyruvate dehydrogenase-e1α deficiency presenting as recurrent demyelination: an unusual presentation and a novel mutationPratibha Singhi, Linda De Meirleir, Willy Lissens, et al.
European Journal of Human Genetics : EJHG|November 29, 2012
A new double substitution mutation in the MEN1 gene: a limited penetrance and a specific phenotypeUrielle Ullmann, David Unuane, Brigitte Velkeniers, et al.
American Journal of Respiratory and Critical Care Medicine|February 26, 2008
A new missense mutation in the CASR gene in familial interstitial lung disease with hypocalciuric hypercalcemia and defective granulocyte functionMaurits Demedts, Willy Lissens, Wim Wuyts, et al.
Human Molecular Genetics|June 5, 2003
Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasiaElisabeth Sock, Roberta A Pagon, Kathelijn Keymolen, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Human Reproduction (Oxford, England)|March 26, 2005
The choice and outcome of the fertility treatment of 38 couples in whom the male partner has a Yq microdeletionKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
Journal of the Neurological Sciences|July 15, 2011
A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperatureVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
European Journal of Human Genetics : EJHG|November 25, 2004
Possible role of USP26 in patients with severely impaired spermatogenesisKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
International Journal of Andrology|November 24, 2006
Alterations of the USP26 gene in Caucasian menKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
Fertility and Sterility|October 11, 2005
SYCP3 mutations are uncommon in patients with azoospermiaKatrien Stouffs, Willy Lissens, Herman Tournaye, et al.
Fertility and Sterility|February 9, 2008
Is there a role for the nuclear export factor 2 gene in male infertility?Katrien Stouffs, Herman Tournaye, Josiane Van der Elst, et al.
JIMD Reports|February 23, 2013
Pyruvate dehydrogenase-e1α deficiency presenting as recurrent demyelination: an unusual presentation and a novel mutationPratibha Singhi, Linda De Meirleir, Willy Lissens, et al.
European Journal of Human Genetics : EJHG|November 29, 2012
A new double substitution mutation in the MEN1 gene: a limited penetrance and a specific phenotypeUrielle Ullmann, David Unuane, Brigitte Velkeniers, et al.
American Journal of Respiratory and Critical Care Medicine|February 26, 2008
A new missense mutation in the CASR gene in familial interstitial lung disease with hypocalciuric hypercalcemia and defective granulocyte functionMaurits Demedts, Willy Lissens, Wim Wuyts, et al.
Human Molecular Genetics|June 5, 2003
Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasiaElisabeth Sock, Roberta A Pagon, Kathelijn Keymolen, et al.
Pageof 7