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E Vamos

Showing results (121-130 of 129) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
Annales De Genetique|March 1, 1976
[Attempt at antenatal diagnosis of argininosuccinic aciduria]J L Dhondt, J P Farriaux, R J Pollitt, et al.
American Journal of Medical Genetics|October 1, 1988
Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibsL Van Maldergem, E Vamos, I Liebaers, et al.
Human Genetics|September 1, 1991
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndromeG Pierquin, N Van Regemorter, Hayez-Delatte, et al.
Animal Microbiome|January 6, 2025
Progression of the faecal microbiome in preweaning dairy calves that develop cryptosporidiosisM F Hares, B E Griffiths, L Barningham, et al.
Human Genetics|December 18, 1998
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversionW Courtens, D Grossman, N Van Roy, et al.
Human Genetics|March 10, 1999
Delineation of two distinct 6p deletion syndromesA F Davies, G Mirza, G Sekhon, et al.
Human Genetics|October 1, 1996
A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndromeA F Davies, M G Olavesen, R J Stephens, et al.
Neurology|January 1, 1992
Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNAH J Tritschler, F Andreetta, C T Moraes, et al.
Pageof 13

Showing results (121-130 of 129) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 129 results.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
Annales De Genetique|March 1, 1976
[Attempt at antenatal diagnosis of argininosuccinic aciduria]J L Dhondt, J P Farriaux, R J Pollitt, et al.
American Journal of Medical Genetics|October 1, 1988
Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibsL Van Maldergem, E Vamos, I Liebaers, et al.
Human Genetics|September 1, 1991
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndromeG Pierquin, N Van Regemorter, Hayez-Delatte, et al.
Animal Microbiome|January 6, 2025
Progression of the faecal microbiome in preweaning dairy calves that develop cryptosporidiosisM F Hares, B E Griffiths, L Barningham, et al.
Human Genetics|December 18, 1998
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversionW Courtens, D Grossman, N Van Roy, et al.
Human Genetics|March 10, 1999
Delineation of two distinct 6p deletion syndromesA F Davies, G Mirza, G Sekhon, et al.
Human Genetics|October 1, 1996
A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndromeA F Davies, M G Olavesen, R J Stephens, et al.
Neurology|January 1, 1992
Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNAH J Tritschler, F Andreetta, C T Moraes, et al.
Pageof 13