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D Nicholls

Showing results (161-170 of 228) with videos related to

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American Journal of Human Genetics|July 11, 1990
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markersJ H Knoll, R D Nicholls, R E Magenis, et al.
Endocrinology|July 9, 2005
Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thriveM Stefan, H Ji, R A Simmons, et al.
International Journal of Obesity (2005)|September 21, 2011
Family-based behavioural treatment of childhood obesity in a UK National Health Service setting: randomized controlled trialH Croker, R M Viner, D Nicholls, et al.
Human Molecular Genetics|April 10, 1999
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical regionM T Jong, T A Gray, Y Ji, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Multiple imprinted genes associated with Prader-Willi syndrome and location of an imprinting control elementR D Nicholls, M T Jong, C C Glenn, et al.
American Journal of Human Genetics|February 1, 1996
Gene structure, DNA methylation, and imprinted expression of the human SNRPN geneC C Glenn, S Saitoh, M T Jong, et al.
Human Molecular Genetics|September 1, 1993
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patientsC C Glenn, R D Nicholls, W P Robinson, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptorC T Culiat, L Stubbs, R D Nicholls, et al.
American Journal of Medical Genetics|July 11, 1997
Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P alleleR A Spritz, T Bailin, R D Nicholls, et al.
Journal of Medical Genetics|January 1, 1987
High resolution gene mapping of the human alpha globin locusR D Nicholls, J A Jonasson, J O McGee, et al.
Pageof 23

Showing results (161-170 of 228) with videos related to

Sort By:
Pageof 23
American Journal of Human Genetics|July 11, 1990
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markersJ H Knoll, R D Nicholls, R E Magenis, et al.
Endocrinology|July 9, 2005
Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thriveM Stefan, H Ji, R A Simmons, et al.
International Journal of Obesity (2005)|September 21, 2011
Family-based behavioural treatment of childhood obesity in a UK National Health Service setting: randomized controlled trialH Croker, R M Viner, D Nicholls, et al.
Human Molecular Genetics|April 10, 1999
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical regionM T Jong, T A Gray, Y Ji, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Multiple imprinted genes associated with Prader-Willi syndrome and location of an imprinting control elementR D Nicholls, M T Jong, C C Glenn, et al.
American Journal of Human Genetics|February 1, 1996
Gene structure, DNA methylation, and imprinted expression of the human SNRPN geneC C Glenn, S Saitoh, M T Jong, et al.
Human Molecular Genetics|September 1, 1993
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patientsC C Glenn, R D Nicholls, W P Robinson, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptorC T Culiat, L Stubbs, R D Nicholls, et al.
American Journal of Medical Genetics|July 11, 1997
Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P alleleR A Spritz, T Bailin, R D Nicholls, et al.
Journal of Medical Genetics|January 1, 1987
High resolution gene mapping of the human alpha globin locusR D Nicholls, J A Jonasson, J O McGee, et al.
Pageof 23