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Sayaka Hashimoto

Showing results (21-30 of 25) with videos related to

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Forensic Science International. Genetics|August 17, 2013
Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridizationElena A Repnikova, Jill A Rosenfeld, Andrea Bailes, et al.
Molecular Genetics & Genomic Medicine|March 25, 2015
A slowly progressive form of limb-girdle muscular dystrophy type 2C associated with founder mutation in the SGCG gene in Puerto Rican HispanicsSamiah A Al-Zaidy, Vinod Malik, Kelley Kneile, et al.
The Journal of Molecular Diagnostics : JMD|June 19, 2022
A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering SpecialtiesMariam T Mathew, Austin Antoniou, Naveen Ramesh, et al.
Cold Spring Harbor Molecular Case Studies|May 7, 2020
Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experienceCecelia R Miller, Kristy Lee, Ruthann B Pfau, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Forensic Science International. Genetics|August 17, 2013
Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridizationElena A Repnikova, Jill A Rosenfeld, Andrea Bailes, et al.
Molecular Genetics & Genomic Medicine|March 25, 2015
A slowly progressive form of limb-girdle muscular dystrophy type 2C associated with founder mutation in the SGCG gene in Puerto Rican HispanicsSamiah A Al-Zaidy, Vinod Malik, Kelley Kneile, et al.
The Journal of Molecular Diagnostics : JMD|June 19, 2022
A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering SpecialtiesMariam T Mathew, Austin Antoniou, Naveen Ramesh, et al.
Cold Spring Harbor Molecular Case Studies|May 7, 2020
Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experienceCecelia R Miller, Kristy Lee, Ruthann B Pfau, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
Pageof 3