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Showing results (81-90 of 89) with videos related to

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Genomics|September 19, 1998
Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyomaR A Lynch, M Piper, A Bankier, et al.
Journal of Medical Genetics|October 1, 1995
Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic featuresA M Estop, P A Mowery-Rushton, K M Cieply, et al.
Clinical Genetics|October 2, 2012
Application of chromosomal microarray in the evaluation of abnormal prenatal findingsS A Yatsenko, S Davis, N W Hendrix, et al.
American Journal of Human Genetics|July 1, 1995
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patientsS L Christian, W P Robinson, B Huang, et al.
The EMBO Journal|March 1, 1988
Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locusJ E Berman, S J Mellis, R Pollock, et al.
Journal of Medical Genetics|August 3, 2006
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative studyM D Graf, L Christ, J T Mascarello, et al.
Prenatal Diagnosis|April 1, 1996
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicismS L Christian, A C Smith, M Macha, et al.
Clinical Genetics|July 9, 2015
High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacyS A Yatsenko, H A Bakos, K Vitullo, et al.
Molecular Neuropsychiatry|November 4, 2015
Genetic and morphological features of human iPSC-derived neurons with chromosome 15q11.2 (BP1-BP2) deletionsD K Das, V Tapias, L D'Aiuto, et al.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
Genomics|September 19, 1998
Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyomaR A Lynch, M Piper, A Bankier, et al.
Journal of Medical Genetics|October 1, 1995
Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic featuresA M Estop, P A Mowery-Rushton, K M Cieply, et al.
Clinical Genetics|October 2, 2012
Application of chromosomal microarray in the evaluation of abnormal prenatal findingsS A Yatsenko, S Davis, N W Hendrix, et al.
American Journal of Human Genetics|July 1, 1995
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patientsS L Christian, W P Robinson, B Huang, et al.
The EMBO Journal|March 1, 1988
Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locusJ E Berman, S J Mellis, R Pollock, et al.
Journal of Medical Genetics|August 3, 2006
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative studyM D Graf, L Christ, J T Mascarello, et al.
Prenatal Diagnosis|April 1, 1996
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicismS L Christian, A C Smith, M Macha, et al.
Clinical Genetics|July 9, 2015
High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacyS A Yatsenko, H A Bakos, K Vitullo, et al.
Molecular Neuropsychiatry|November 4, 2015
Genetic and morphological features of human iPSC-derived neurons with chromosome 15q11.2 (BP1-BP2) deletionsD K Das, V Tapias, L D'Aiuto, et al.
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