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G L Feldman

Showing results (31-40 of 56) with videos related to

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Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|September 11, 1975
The influence of exogenous PMS and HCG on the arachidonic acid content of the immature rat ovaryH T Jonsson, T W Culp, R H Kaufman, et al.
Journal of Pediatric and Adolescent Gynecology|November 1, 1996
An association between precocious puberty and fragile X syndrome?C L Kowalczyk, E Schroeder, V Pratt, et al.
American Journal of Human Genetics|March 1, 1989
Linkage disequilibrium, cystic fibrosis, and genetic counselingA L Beaudet, G L Feldman, S D Fernbach, et al.
American Journal of Medical Genetics|September 15, 1993
Inverted duplication of 8p: ten new patients and review of the literatureG L Feldman, L Weiss, M C Phelan, et al.
American Journal of Medical Genetics|December 1, 1993
Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridizationJ L Zenger-Hain, D L Van Dyke, A Wiktor, et al.
Human Molecular Genetics|March 1, 1995
Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndromeF Z Bischoff, G L Feldman, C McCaskill, et al.
American Journal of Medical Genetics|February 24, 2001
Frequency and clinical significance of the S1235R mutation in the cystic fibrosis transmembrane conductance regulator gene: results from a collaborative studyK G Monaghan, G L Feldman, G M Barbarotto, et al.
American Journal of Medical Genetics|April 24, 1999
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomyS A Berend, G L Feldman, C McCaskill, et al.
American Journal of Ophthalmology|October 1, 1995
Relationship of familial prominent corneal nerves and lesions of the tongue resembling neuromas to multiple endocrine neoplasia type 2BP J Dennehy, G L Feldman, M Kambouris, et al.
American Journal of Human Genetics|July 1, 1997
DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear geneV M Pratt, C E Jackson, D C Wallace, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|September 11, 1975
The influence of exogenous PMS and HCG on the arachidonic acid content of the immature rat ovaryH T Jonsson, T W Culp, R H Kaufman, et al.
Journal of Pediatric and Adolescent Gynecology|November 1, 1996
An association between precocious puberty and fragile X syndrome?C L Kowalczyk, E Schroeder, V Pratt, et al.
American Journal of Human Genetics|March 1, 1989
Linkage disequilibrium, cystic fibrosis, and genetic counselingA L Beaudet, G L Feldman, S D Fernbach, et al.
American Journal of Medical Genetics|September 15, 1993
Inverted duplication of 8p: ten new patients and review of the literatureG L Feldman, L Weiss, M C Phelan, et al.
American Journal of Medical Genetics|December 1, 1993
Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridizationJ L Zenger-Hain, D L Van Dyke, A Wiktor, et al.
Human Molecular Genetics|March 1, 1995
Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndromeF Z Bischoff, G L Feldman, C McCaskill, et al.
American Journal of Medical Genetics|February 24, 2001
Frequency and clinical significance of the S1235R mutation in the cystic fibrosis transmembrane conductance regulator gene: results from a collaborative studyK G Monaghan, G L Feldman, G M Barbarotto, et al.
American Journal of Medical Genetics|April 24, 1999
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomyS A Berend, G L Feldman, C McCaskill, et al.
American Journal of Ophthalmology|October 1, 1995
Relationship of familial prominent corneal nerves and lesions of the tongue resembling neuromas to multiple endocrine neoplasia type 2BP J Dennehy, G L Feldman, M Kambouris, et al.
American Journal of Human Genetics|July 1, 1997
DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear geneV M Pratt, C E Jackson, D C Wallace, et al.
Pageof 6