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Nature
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October 10, 1985
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
S T Reeders, M H Breuning, K E Davies, et al.
British Journal of Haematology
|
July 1, 1995
The myelodysplastic syndromes: an analysis of prognostic factors in 226 cases from a single institution
I Cunningham, S J MacCallum, M D Nicholls, et al.
American Journal of Human Genetics
|
June 15, 2007
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency
M He, S L Rutledge, D R Kelly, et al.
American Journal of Medical Genetics
|
May 1, 1989
Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome
U Tantravahi, R D Nicholls, H Stroh, et al.
American Journal of Human Genetics
|
September 26, 2003
Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons
J-H Chai, D P Locke, J M Greally, et al.
American Journal of Medical Genetics. Part A
|
May 5, 2021
Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approach
Rachel M Wolfe, Al-Walid Mohsen, Cate Walsh Vockley, et al.
American Journal of Human Genetics
|
January 14, 2005
Possible genomic imprinting of three human obesity-related genetic loci
Chuanhui Dong, Wei-Dong Li, Frank Geller, et al.
American Journal of Medical Genetics
|
May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome
R D Nicholls, J H Knoll, K Glatt, et al.
Genomics
|
June 14, 2000
The ancient source of a distinct gene family encoding proteins featuring RING and C(3)H zinc-finger motifs with abundant expression in developing brain and nervous system
T A Gray, L Hernandez, A H Carey, et al.
Nature
|
January 7, 1993
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism
E M Rinchik, S J Bultman, B Horsthemke, et al.
Page
of 23
Search research articles
Search
Showing results (191-200 of 228) with videos related to
Sort By:
Page
of 23
Nature
|
October 10, 1985
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
S T Reeders, M H Breuning, K E Davies, et al.
British Journal of Haematology
|
July 1, 1995
The myelodysplastic syndromes: an analysis of prognostic factors in 226 cases from a single institution
I Cunningham, S J MacCallum, M D Nicholls, et al.
American Journal of Human Genetics
|
June 15, 2007
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency
M He, S L Rutledge, D R Kelly, et al.
American Journal of Medical Genetics
|
May 1, 1989
Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome
U Tantravahi, R D Nicholls, H Stroh, et al.
American Journal of Human Genetics
|
September 26, 2003
Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons
J-H Chai, D P Locke, J M Greally, et al.
American Journal of Medical Genetics. Part A
|
May 5, 2021
Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approach
Rachel M Wolfe, Al-Walid Mohsen, Cate Walsh Vockley, et al.
American Journal of Human Genetics
|
January 14, 2005
Possible genomic imprinting of three human obesity-related genetic loci
Chuanhui Dong, Wei-Dong Li, Frank Geller, et al.
American Journal of Medical Genetics
|
May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome
R D Nicholls, J H Knoll, K Glatt, et al.
Genomics
|
June 14, 2000
The ancient source of a distinct gene family encoding proteins featuring RING and C(3)H zinc-finger motifs with abundant expression in developing brain and nervous system
T A Gray, L Hernandez, A H Carey, et al.
Nature
|
January 7, 1993
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism
E M Rinchik, S J Bultman, B Horsthemke, et al.
Page
of 23