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L G Shaffer

Showing results (71-80 of 133) with videos related to

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American Journal of Human Genetics|October 6, 2000
Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndromeY Q Wu, J L Badano, C McCaskill, et al.
American Journal of Medical Genetics|December 14, 1999
De novo direct duplication of 15q15-->q24 in a newborn boy with mild manifestationsJ Y Han, K H Kim, H D Lee, et al.
American Journal of Medical Genetics|December 1, 1993
Prenatal diagnosis and clinical findings in a case of hexasomy 12pI B Van den Veyver, M E Macha, C McCaskill, et al.
Human Genetics|February 1, 1991
A molecular genetic approach to the identification of isochromosomes of chromosome 21L G Shaffer, C K Jackson-Cook, J M Meyer, et al.
Human Genetics|October 30, 1999
Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor geneK R Bowles, J Gibson, J Wu, et al.
Human Molecular Genetics|March 1, 1995
Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndromeF Z Bischoff, G L Feldman, C McCaskill, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Array comparative genomic hybridization in global developmental delayM I Shevell, B A Bejjani, M Srour, et al.
American Journal of Medical Genetics|March 27, 1995
Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted regionE A Lindsay, F Greenberg, L G Shaffer, et al.
American Journal of Medical Genetics|August 1, 1992
Parental origin determination in thirty de novo Robertsonian translocationsL G Shaffer, C K Jackson-Cook, B A Stasiowski, et al.
American Journal of Medical Genetics|April 24, 1999
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomyS A Berend, G L Feldman, C McCaskill, et al.
Pageof 14

Showing results (71-80 of 133) with videos related to

Sort By:
Pageof 14
American Journal of Human Genetics|October 6, 2000
Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndromeY Q Wu, J L Badano, C McCaskill, et al.
American Journal of Medical Genetics|December 14, 1999
De novo direct duplication of 15q15-->q24 in a newborn boy with mild manifestationsJ Y Han, K H Kim, H D Lee, et al.
American Journal of Medical Genetics|December 1, 1993
Prenatal diagnosis and clinical findings in a case of hexasomy 12pI B Van den Veyver, M E Macha, C McCaskill, et al.
Human Genetics|February 1, 1991
A molecular genetic approach to the identification of isochromosomes of chromosome 21L G Shaffer, C K Jackson-Cook, J M Meyer, et al.
Human Genetics|October 30, 1999
Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor geneK R Bowles, J Gibson, J Wu, et al.
Human Molecular Genetics|March 1, 1995
Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndromeF Z Bischoff, G L Feldman, C McCaskill, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Array comparative genomic hybridization in global developmental delayM I Shevell, B A Bejjani, M Srour, et al.
American Journal of Medical Genetics|March 27, 1995
Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted regionE A Lindsay, F Greenberg, L G Shaffer, et al.
American Journal of Medical Genetics|August 1, 1992
Parental origin determination in thirty de novo Robertsonian translocationsL G Shaffer, C K Jackson-Cook, B A Stasiowski, et al.
American Journal of Medical Genetics|April 24, 1999
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomyS A Berend, G L Feldman, C McCaskill, et al.
Pageof 14