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Showing results (31-40 of 35) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|March 23, 2016
Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian InsufficiencyC Hyon, L Mansour-Hendili, S Chantot-Bastaraud, et al.
Human Molecular Genetics|December 1, 1996
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutationsI Mansour, V Delague, C Cazeneuve, et al.
Human Molecular Genetics|July 21, 1998
Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF)A Bernot, C da Silva, J L Petit, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
The Journal of Clinical Endocrinology and Metabolism|March 23, 2016
Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian InsufficiencyC Hyon, L Mansour-Hendili, S Chantot-Bastaraud, et al.
Human Molecular Genetics|December 1, 1996
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutationsI Mansour, V Delague, C Cazeneuve, et al.
Human Molecular Genetics|July 21, 1998
Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF)A Bernot, C da Silva, J L Petit, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Pageof 4