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M G Butler

Showing results (171-180 of 212) with videos related to

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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.
Cancer Genetics and Cytogenetics|September 2, 1998
Comparison of chromosome telomere integrity in multiple tissues from subjects at different agesM G Butler, J Tilburt, A DeVries, et al.
British Heart Journal|October 1, 1986
Isolated atrial amyloid contains atrial natriuretic peptide: a report of six casesG C Kaye, M G Butler, A J d'Ardenne, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1991
Hereditary lymphedema and distichiasisT Kolin, K J Johns, W B Wadlington, et al.
Cytogenetic and Genome Research|May 8, 2009
Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGHD C Bittel, S Yu, H Newkirk, et al.
Cancer Genetics and Cytogenetics|August 5, 1998
Clear cell sarcoma or malignant melanoma of soft parts: molecular analysis of microsatellite instability with clinical correlationG Aue, L K Hedges, H S Schwartz, et al.
Journal of Medical Genetics|May 2, 2006
Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autismZ Talebizadeh, D Y Lam, M F Theodoro, et al.
Clinical Genetics|May 20, 2003
Five new subjects with ring chromosome 22H A Ishmael, D Cataldi, M L Begleiter, et al.
Journal of Medical Genetics|November 5, 2002
No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)Z Talebizadeh, D C Bittel, J H Miles, et al.
American Journal of Respiratory and Critical Care Medicine|July 1, 1995
Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertensionJ E Loyd, M G Butler, T M Foroud, et al.
Pageof 22

Showing results (171-180 of 212) with videos related to

Sort By:
Pageof 22
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.
Cancer Genetics and Cytogenetics|September 2, 1998
Comparison of chromosome telomere integrity in multiple tissues from subjects at different agesM G Butler, J Tilburt, A DeVries, et al.
British Heart Journal|October 1, 1986
Isolated atrial amyloid contains atrial natriuretic peptide: a report of six casesG C Kaye, M G Butler, A J d'Ardenne, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1991
Hereditary lymphedema and distichiasisT Kolin, K J Johns, W B Wadlington, et al.
Cytogenetic and Genome Research|May 8, 2009
Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGHD C Bittel, S Yu, H Newkirk, et al.
Cancer Genetics and Cytogenetics|August 5, 1998
Clear cell sarcoma or malignant melanoma of soft parts: molecular analysis of microsatellite instability with clinical correlationG Aue, L K Hedges, H S Schwartz, et al.
Journal of Medical Genetics|May 2, 2006
Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autismZ Talebizadeh, D Y Lam, M F Theodoro, et al.
Clinical Genetics|May 20, 2003
Five new subjects with ring chromosome 22H A Ishmael, D Cataldi, M L Begleiter, et al.
Journal of Medical Genetics|November 5, 2002
No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)Z Talebizadeh, D C Bittel, J H Miles, et al.
American Journal of Respiratory and Critical Care Medicine|July 1, 1995
Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertensionJ E Loyd, M G Butler, T M Foroud, et al.
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