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Showing results (71-80 of 78) with videos related to

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Journal of Medical Genetics|September 10, 2003
Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarraysH Fiegler, S M Gribble, D C Burford, et al.
Cytogenetic and Genome Research|July 21, 2009
Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1A C V Krepischi-Santos, D Rajan, I K Temple, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Pancreatic hypoplasia presenting with neonatal diabetes mellitus in association with congenital heart defect and developmental delayM Balasubramanian, J P H Shield, C L Acerini, et al.
The British Journal of Ophthalmology|May 25, 2007
SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletionsP Bakrania, D O Robinson, D J Bunyan, et al.
Journal of Medical Genetics|January 7, 2005
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypesS M Gribble, E Prigmore, D C Burford, et al.
American Journal of Human Genetics|April 25, 2000
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromereP E Warburton, M Dolled, R Mahmood, et al.
European Journal of Medical Genetics|April 24, 2012
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardationE K Bijlsma, A Collins, F T Papa, et al.
Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Journal of Medical Genetics|September 10, 2003
Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarraysH Fiegler, S M Gribble, D C Burford, et al.
Cytogenetic and Genome Research|July 21, 2009
Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1A C V Krepischi-Santos, D Rajan, I K Temple, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Pancreatic hypoplasia presenting with neonatal diabetes mellitus in association with congenital heart defect and developmental delayM Balasubramanian, J P H Shield, C L Acerini, et al.
The British Journal of Ophthalmology|May 25, 2007
SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletionsP Bakrania, D O Robinson, D J Bunyan, et al.
Journal of Medical Genetics|January 7, 2005
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypesS M Gribble, E Prigmore, D C Burford, et al.
American Journal of Human Genetics|April 25, 2000
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromereP E Warburton, M Dolled, R Mahmood, et al.
European Journal of Medical Genetics|April 24, 2012
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardationE K Bijlsma, A Collins, F T Papa, et al.
Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.
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