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Trilochan Sahoo

Showing results (21-30 of 65) with videos related to

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Clinical Dysmorphology|October 10, 2020
Heterozygous intragenic deletions of FREM1 are not associated with trigonocephalyAngelika J Dawson, Karine Hovanes, Jing Liu, et al.
American Journal of Medical Genetics. Part A|March 8, 2026
Unusual Recombinant Chromosome 6 Derived From a Parental Rearrangement With Complex Paracentric InversionsMelanie Babcock, Marwa Daghsni, Jessica Sebastian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disordersJill A Rosenfeld, Blake C Ballif, Beth S Torchia, et al.
Molecular Cytogenetics|May 4, 2013
Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature reviewMorteza Hemmat, Omid Hemmat, Arturo Anguiano, et al.
Nature Genetics|May 27, 2008
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterTrilochan Sahoo, Daniela del Gaudio, Jennifer R German, et al.
European Journal of Human Genetics : EJHG|May 25, 2007
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlationsTrilochan Sahoo, Carlos A Bacino, Jennifer R German, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesityMarwan Shinawi, Trilochan Sahoo, Bruno Maranda, et al.
American Journal of Medical Genetics. Part A|June 15, 2011
Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palateTrilochan Sahoo, Aaron Theisen, Pedro A Sanchez-Lara, et al.
Prenatal Diagnosis|September 17, 2008
Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGHWeimin Bi, Amy M Breman, Susan F Venable, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomaliesDaniel R Jensen, Donna M Martin, Stephen Gebarski, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Clinical Dysmorphology|October 10, 2020
Heterozygous intragenic deletions of FREM1 are not associated with trigonocephalyAngelika J Dawson, Karine Hovanes, Jing Liu, et al.
American Journal of Medical Genetics. Part A|March 8, 2026
Unusual Recombinant Chromosome 6 Derived From a Parental Rearrangement With Complex Paracentric InversionsMelanie Babcock, Marwa Daghsni, Jessica Sebastian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disordersJill A Rosenfeld, Blake C Ballif, Beth S Torchia, et al.
Molecular Cytogenetics|May 4, 2013
Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature reviewMorteza Hemmat, Omid Hemmat, Arturo Anguiano, et al.
Nature Genetics|May 27, 2008
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterTrilochan Sahoo, Daniela del Gaudio, Jennifer R German, et al.
European Journal of Human Genetics : EJHG|May 25, 2007
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlationsTrilochan Sahoo, Carlos A Bacino, Jennifer R German, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesityMarwan Shinawi, Trilochan Sahoo, Bruno Maranda, et al.
American Journal of Medical Genetics. Part A|June 15, 2011
Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palateTrilochan Sahoo, Aaron Theisen, Pedro A Sanchez-Lara, et al.
Prenatal Diagnosis|September 17, 2008
Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGHWeimin Bi, Amy M Breman, Susan F Venable, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomaliesDaniel R Jensen, Donna M Martin, Stephen Gebarski, et al.
Pageof 7