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W Scherer

Showing results (521-530 of 915) with videos related to

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Genomics|July 15, 1994
Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clonesJ Kunz, S W Scherer, I Klawitz, et al.
American Journal of Human Genetics|June 1, 1995
Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patientT L Alley, B A Gray, S H Lee, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndromeMehdi Zarrei, Daniele Merico, Barbara Kellam, et al.
Human Mutation|April 18, 2015
15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric PhenotypesAbdul Noor, Lucie Dupuis, Kirti Mittal, et al.
European Journal of Human Genetics : EJHG|July 7, 2018
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesityThanuja Selvanayagam, Susan Walker, Matthew J Gazzellone, et al.
Cytogenetics and Cell Genetics|November 4, 2000
Human secretin (SCT): gene structure, chromosome location, and distribution of mRNAT E Whitmore, J L Holloway, C E Lofton-Day, et al.
Plos One|December 24, 2014
Extent of non-publication in cohorts of studies approved by research ethics committees or included in trial registriesChristine Schmucker, Lisa K Schell, Susan Portalupi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 21, 2017
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysisYanqing Zhang, Yi Liu, Mehdi Zarrei, et al.
Fertility and Sterility|January 28, 2014
Development of a high-resolution Y-chromosome microarray for improved male infertility diagnosisRyan K C Yuen, Anna Merkoulovitch, Jeffrey R MacDonald, et al.
Scientific Reports|July 27, 2025
Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencingRui Guo, Chunhong Duan, Mehdi Zarrei, et al.
Pageof 92

Showing results (521-530 of 915) with videos related to

Sort By:
Pageof 92
Genomics|July 15, 1994
Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clonesJ Kunz, S W Scherer, I Klawitz, et al.
American Journal of Human Genetics|June 1, 1995
Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patientT L Alley, B A Gray, S H Lee, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndromeMehdi Zarrei, Daniele Merico, Barbara Kellam, et al.
Human Mutation|April 18, 2015
15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric PhenotypesAbdul Noor, Lucie Dupuis, Kirti Mittal, et al.
European Journal of Human Genetics : EJHG|July 7, 2018
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesityThanuja Selvanayagam, Susan Walker, Matthew J Gazzellone, et al.
Cytogenetics and Cell Genetics|November 4, 2000
Human secretin (SCT): gene structure, chromosome location, and distribution of mRNAT E Whitmore, J L Holloway, C E Lofton-Day, et al.
Plos One|December 24, 2014
Extent of non-publication in cohorts of studies approved by research ethics committees or included in trial registriesChristine Schmucker, Lisa K Schell, Susan Portalupi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 21, 2017
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysisYanqing Zhang, Yi Liu, Mehdi Zarrei, et al.
Fertility and Sterility|January 28, 2014
Development of a high-resolution Y-chromosome microarray for improved male infertility diagnosisRyan K C Yuen, Anna Merkoulovitch, Jeffrey R MacDonald, et al.
Scientific Reports|July 27, 2025
Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencingRui Guo, Chunhong Duan, Mehdi Zarrei, et al.
Pageof 92