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Stuart Schwartz

Showing results (41-50 of 73) with videos related to

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Oncogene|February 22, 2002
Chromosomal autonomy of hMLH1 methylation in colon cancerHui Li, Lois Myeroff, Lakshmi Kasturi, et al.
European Journal of Medical Genetics|November 17, 2010
Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotypeShalini C Reshmi, Jennifer L Miller, Dianne Deplewski, et al.
Prenatal Diagnosis|March 29, 2002
Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probesMark J Pettenati, Chris Von Kap-Herr, Bethy Jackle, et al.
Human Genetics|February 10, 2004
Delineation of complex chromosomal rearrangements: evidence for increased complexityCaroline Astbury, Laurie A Christ, David J Aughton, et al.
Pediatrics|August 3, 2004
Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrumMelanie A Manning, Suzanne B Cassidy, Carol Clericuzio, et al.
Statistics in Medicine|January 29, 2005
Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practicesSamuel P Caudill, Daniel L Van Dyke, Andrew T L Chen, et al.
American Journal of Human Genetics|December 4, 2001
Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22Jeffrey A Bailey, Amy M Yavor, Luigi Viggiano, et al.
Science (New York, N.Y.)|June 8, 2002
Covariation of synaptonemal complex length and mammalian meiotic exchange ratesAudrey Lynn, Kara E Koehler, LuAnn Judis, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
UPD detection using homozygosity profiling with a SNP genotyping microarrayPeter Papenhausen, Stuart Schwartz, Hiba Risheg, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearanceMałgorzata J M Nowaczyk, Melissa T Carter, Jie Xu, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
Oncogene|February 22, 2002
Chromosomal autonomy of hMLH1 methylation in colon cancerHui Li, Lois Myeroff, Lakshmi Kasturi, et al.
European Journal of Medical Genetics|November 17, 2010
Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotypeShalini C Reshmi, Jennifer L Miller, Dianne Deplewski, et al.
Prenatal Diagnosis|March 29, 2002
Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probesMark J Pettenati, Chris Von Kap-Herr, Bethy Jackle, et al.
Human Genetics|February 10, 2004
Delineation of complex chromosomal rearrangements: evidence for increased complexityCaroline Astbury, Laurie A Christ, David J Aughton, et al.
Pediatrics|August 3, 2004
Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrumMelanie A Manning, Suzanne B Cassidy, Carol Clericuzio, et al.
Statistics in Medicine|January 29, 2005
Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practicesSamuel P Caudill, Daniel L Van Dyke, Andrew T L Chen, et al.
American Journal of Human Genetics|December 4, 2001
Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22Jeffrey A Bailey, Amy M Yavor, Luigi Viggiano, et al.
Science (New York, N.Y.)|June 8, 2002
Covariation of synaptonemal complex length and mammalian meiotic exchange ratesAudrey Lynn, Kara E Koehler, LuAnn Judis, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
UPD detection using homozygosity profiling with a SNP genotyping microarrayPeter Papenhausen, Stuart Schwartz, Hiba Risheg, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearanceMałgorzata J M Nowaczyk, Melissa T Carter, Jie Xu, et al.
Pageof 8