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Taneli Raivio

Showing results (131-140 of 135) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|February 10, 2012
Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasiaTaneli Raivio, Magdalena Avbelj, Mark J McCabe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2014
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutationsCarine Villanueva, Elka Jacobson-Dickman, Cheng Xu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 23, 2013
Hereditary myopathy with early respiratory failure: occurrence in various populationsJohanna Palmio, Anni Evilä, Françoise Chapon, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
Nature Communications|November 4, 2017
Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosisJohanna Tommiska, Johanna Känsäkoski, Lasse Skibsbye, et al.
Pageof 14

Showing results (131-140 of 135) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 135 results.
The Journal of Clinical Endocrinology and Metabolism|February 10, 2012
Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasiaTaneli Raivio, Magdalena Avbelj, Mark J McCabe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2014
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutationsCarine Villanueva, Elka Jacobson-Dickman, Cheng Xu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 23, 2013
Hereditary myopathy with early respiratory failure: occurrence in various populationsJohanna Palmio, Anni Evilä, Françoise Chapon, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
Nature Communications|November 4, 2017
Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosisJohanna Tommiska, Johanna Känsäkoski, Lasse Skibsbye, et al.
Pageof 14