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L G Shaffer

Showing results (101-110 of 133) with videos related to

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Genomics|April 28, 2000
Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genesB E Tubb, S Bardien-Kruger, C D Kashork, et al.
Journal of Medical Genetics|June 14, 2000
Circadian rhythm abnormalities of melatonin in Smith-Magenis syndromeL Potocki, D Glaze, D X Tan, et al.
Nature Genetics|November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXEJ E Parrish, B A Oostra, A J Verkerk, et al.
American Journal of Medical Genetics|November 11, 1996
Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11)C A Walter, L G Shaffer, C I Kaye, et al.
American Journal of Human Genetics|November 1, 1994
Molecular characterization of de novo secondary trisomy 13L G Shaffer, C McCaskill, J Y Han, et al.
American Journal of Medical Genetics|June 24, 1998
Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental originY Q Wu, V R Sutton, E Nickerson, et al.
American Journal of Human Genetics|October 27, 1997
Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndromeS K Shapira, C McCaskill, H Northrup, et al.
Human Molecular Genetics|February 5, 1999
Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletionsY Q Wu, H A Heilstedt, J A Bedell, et al.
Human Mutation|June 20, 2003
Epigenetic detection of human chromosome 14 uniparental disomyS K Murphy, A A Wylie, K J Coveler, et al.
Human Molecular Genetics|December 23, 1999
Poly(ADP-ribose) polymerase at active centromeres and neocentromeres at metaphaseE Earle, A Saxena, A MacDonald, et al.
Pageof 14

Showing results (101-110 of 133) with videos related to

Sort By:
Pageof 14
Genomics|April 28, 2000
Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genesB E Tubb, S Bardien-Kruger, C D Kashork, et al.
Journal of Medical Genetics|June 14, 2000
Circadian rhythm abnormalities of melatonin in Smith-Magenis syndromeL Potocki, D Glaze, D X Tan, et al.
Nature Genetics|November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXEJ E Parrish, B A Oostra, A J Verkerk, et al.
American Journal of Medical Genetics|November 11, 1996
Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11)C A Walter, L G Shaffer, C I Kaye, et al.
American Journal of Human Genetics|November 1, 1994
Molecular characterization of de novo secondary trisomy 13L G Shaffer, C McCaskill, J Y Han, et al.
American Journal of Medical Genetics|June 24, 1998
Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental originY Q Wu, V R Sutton, E Nickerson, et al.
American Journal of Human Genetics|October 27, 1997
Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndromeS K Shapira, C McCaskill, H Northrup, et al.
Human Molecular Genetics|February 5, 1999
Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletionsY Q Wu, H A Heilstedt, J A Bedell, et al.
Human Mutation|June 20, 2003
Epigenetic detection of human chromosome 14 uniparental disomyS K Murphy, A A Wylie, K J Coveler, et al.
Human Molecular Genetics|December 23, 1999
Poly(ADP-ribose) polymerase at active centromeres and neocentromeres at metaphaseE Earle, A Saxena, A MacDonald, et al.
Pageof 14