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J Steffann

Showing results (1-10 of 31) with videos related to

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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|August 24, 2010
[Mitochondria and oocyte maturation]J Steffann, C Fallet
Ophthalmic Paediatrics and Genetics|April 1, 1985
Familial congenital cataract, non-progressive neurological disorders and mental deficiency: a new X-linked syndrome?R A Pfeiffer, J Steffann
Clinical Genetics|December 20, 2014
mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal developmentJ Steffann, S Monnot, J-P Bonnefont
The British Journal of Dermatology|October 28, 2017
Postzygotic mosaicism and incontinentia pigmenti in male patients: molecular diagnosis yieldZ Alabdullatif, J Coulombe, J Steffann, et al.
Human Reproduction (Oxford, England)|October 4, 2005
Myotonic dystrophy: does it affect ovarian follicular status and responsiveness to controlled ovarian stimulation?E Feyereisen, A Amar, V Kerbrat, et al.
Annales De Genetique|January 9, 1999
Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileusJ Steffann, D Vidaud, S Bousquet, et al.
Human Reproduction (Oxford, England)|February 29, 2024
What importance do donors and recipients attribute to the nuclear DNA-related genetic heritage of oocyte donation?A Mayeur, F Magnan, S Mathieu, et al.
Gynecologie, Obstetrique & Fertilite|September 6, 2005
[Extending preimplantation genetic diagnosis to HLA typing: the Paris experience]J Steffann, N Frydman, P Burlet, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|November 22, 2018
Increased incidence of obstetric complications in women carrying mitochondrial DNA mutations: a retrospective cohort study in a single tertiary centreM Kuleva, S Ben Miled, J Steffann, et al.
Clinical Genetics|March 18, 2004
Novel CFTR mutations in black cystic fibrosis patientsM N Feuillet-Fieux, M Ferrec, N Gigarel, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|August 24, 2010
[Mitochondria and oocyte maturation]J Steffann, C Fallet
Ophthalmic Paediatrics and Genetics|April 1, 1985
Familial congenital cataract, non-progressive neurological disorders and mental deficiency: a new X-linked syndrome?R A Pfeiffer, J Steffann
Clinical Genetics|December 20, 2014
mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal developmentJ Steffann, S Monnot, J-P Bonnefont
The British Journal of Dermatology|October 28, 2017
Postzygotic mosaicism and incontinentia pigmenti in male patients: molecular diagnosis yieldZ Alabdullatif, J Coulombe, J Steffann, et al.
Human Reproduction (Oxford, England)|October 4, 2005
Myotonic dystrophy: does it affect ovarian follicular status and responsiveness to controlled ovarian stimulation?E Feyereisen, A Amar, V Kerbrat, et al.
Annales De Genetique|January 9, 1999
Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileusJ Steffann, D Vidaud, S Bousquet, et al.
Human Reproduction (Oxford, England)|February 29, 2024
What importance do donors and recipients attribute to the nuclear DNA-related genetic heritage of oocyte donation?A Mayeur, F Magnan, S Mathieu, et al.
Gynecologie, Obstetrique & Fertilite|September 6, 2005
[Extending preimplantation genetic diagnosis to HLA typing: the Paris experience]J Steffann, N Frydman, P Burlet, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|November 22, 2018
Increased incidence of obstetric complications in women carrying mitochondrial DNA mutations: a retrospective cohort study in a single tertiary centreM Kuleva, S Ben Miled, J Steffann, et al.
Clinical Genetics|March 18, 2004
Novel CFTR mutations in black cystic fibrosis patientsM N Feuillet-Fieux, M Ferrec, N Gigarel, et al.
Pageof 4