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R D Nicholls

Showing results (51-60 of 107) with videos related to

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American Journal of Medical Genetics|February 11, 1997
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15S B Cassidy, M Forsythe, S Heeger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 7B C Holdener, S D Brown, J M Angel, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
American Journal of Medical Genetics|July 15, 1992
Pericentric inversion of chromosome 16 in a large kindred: spectrum of morbidity and mortality in offspringD W Bianchi, R D Nicholls, K A Russell, et al.
American Journal of Medical Genetics|February 1, 1989
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionJ H Knoll, R D Nicholls, R E Magenis, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 9, 1998
A model system to study genomic imprinting of human genesJ M Gabriel, M J Higgins, T C Gebuhr, et al.
Genome Research|March 18, 2000
Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in humanY Ji, N A Rebert, J M Joslin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 1998
Genetic mapping of the galanin-GMAP (Galn) gene to mouse chromosome 19L C Guida, P Charlton, D J Gilbert, et al.
American Journal of Human Genetics|August 1, 1996
Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomyL M White, P K Rogan, R D Nicholls, et al.
Nature|July 29, 1993
Allele-specific replication timing of imprinted gene regionsD Kitsberg, S Selig, M Brandeis, et al.
Pageof 11

Showing results (51-60 of 107) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|February 11, 1997
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15S B Cassidy, M Forsythe, S Heeger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 7B C Holdener, S D Brown, J M Angel, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
American Journal of Medical Genetics|July 15, 1992
Pericentric inversion of chromosome 16 in a large kindred: spectrum of morbidity and mortality in offspringD W Bianchi, R D Nicholls, K A Russell, et al.
American Journal of Medical Genetics|February 1, 1989
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionJ H Knoll, R D Nicholls, R E Magenis, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 9, 1998
A model system to study genomic imprinting of human genesJ M Gabriel, M J Higgins, T C Gebuhr, et al.
Genome Research|March 18, 2000
Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in humanY Ji, N A Rebert, J M Joslin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 1998
Genetic mapping of the galanin-GMAP (Galn) gene to mouse chromosome 19L C Guida, P Charlton, D J Gilbert, et al.
American Journal of Human Genetics|August 1, 1996
Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomyL M White, P K Rogan, R D Nicholls, et al.
Nature|July 29, 1993
Allele-specific replication timing of imprinted gene regionsD Kitsberg, S Selig, M Brandeis, et al.
Pageof 11