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S Sparkes

Showing results (131-140 of 355) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1978
Human PGM2 (E.C. 2.7.5.1) mapped to 4pter leads to 4q25R S Sparkes, T Mohandas, M C Sparkes, et al.
Journal of Medical Genetics|April 1, 1982
Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocationK Taysi, R S Sparkes, T J O'Brien, et al.
Clinical Genetics|January 1, 1973
Concurrence of myotonic dystrophy and XXY Klinefelter syndromeR S Sparkes, L Samec, S A Kaplan, et al.
American Journal of Ophthalmology|February 15, 1986
Genetic linkage analysis of autosomal dominant congenital cataractsJ B Bateman, M A Spence, M L Marazita, et al.
Cancer Genetics and Cytogenetics|March 1, 1983
Chromosomal abnormalities of a mediastinal embryonal cell carcinoma in a patient with 47,XXY Klinefelter syndrome: evidence for the premeiotic origin of a germ cell tumorB D Mann, R S Sparkes, D H Kern, et al.
Clinical Genetics|August 1, 1977
Insertional translocation into the X chromosome of a 46,XY maleR S Sparkes, W J Salter, R G Blaker, et al.
Genomics|September 1, 1993
Assignment of the human Na+/glucose cotransporter gene SGLT1 to chromosome 22q13.1E Turk, I Klisak, R Bacallao, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1979
Hemoglobin polymorphism in Equus przewalskii and E. caballus analyzed by isoelectric focusingO A Ryder, R S Sparkes, M C Sparkes, et al.
Annales De Genetique|January 1, 1981
Balanced reciprocal (X;9) translocation in a girl with primary amenorrheaI Leddet-Chevallier, R A Reid, R E Carrel, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 1, 1987
The Rieger syndrome and a chromosome 13 deletionR A Stathacopoulos, J B Bateman, R S Sparkes, et al.
Pageof 36

Showing results (131-140 of 355) with videos related to

Sort By:
Pageof 36
Cytogenetics and Cell Genetics|January 1, 1978
Human PGM2 (E.C. 2.7.5.1) mapped to 4pter leads to 4q25R S Sparkes, T Mohandas, M C Sparkes, et al.
Journal of Medical Genetics|April 1, 1982
Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocationK Taysi, R S Sparkes, T J O'Brien, et al.
Clinical Genetics|January 1, 1973
Concurrence of myotonic dystrophy and XXY Klinefelter syndromeR S Sparkes, L Samec, S A Kaplan, et al.
American Journal of Ophthalmology|February 15, 1986
Genetic linkage analysis of autosomal dominant congenital cataractsJ B Bateman, M A Spence, M L Marazita, et al.
Cancer Genetics and Cytogenetics|March 1, 1983
Chromosomal abnormalities of a mediastinal embryonal cell carcinoma in a patient with 47,XXY Klinefelter syndrome: evidence for the premeiotic origin of a germ cell tumorB D Mann, R S Sparkes, D H Kern, et al.
Clinical Genetics|August 1, 1977
Insertional translocation into the X chromosome of a 46,XY maleR S Sparkes, W J Salter, R G Blaker, et al.
Genomics|September 1, 1993
Assignment of the human Na+/glucose cotransporter gene SGLT1 to chromosome 22q13.1E Turk, I Klisak, R Bacallao, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1979
Hemoglobin polymorphism in Equus przewalskii and E. caballus analyzed by isoelectric focusingO A Ryder, R S Sparkes, M C Sparkes, et al.
Annales De Genetique|January 1, 1981
Balanced reciprocal (X;9) translocation in a girl with primary amenorrheaI Leddet-Chevallier, R A Reid, R E Carrel, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 1, 1987
The Rieger syndrome and a chromosome 13 deletionR A Stathacopoulos, J B Bateman, R S Sparkes, et al.
Pageof 36