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Prenatal Diagnosis
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February 27, 2024
Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical study
Michelle Bellair, Elisabete Amaral, Mason Ouren, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2004
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A
Yong-Hui Jiang, Trilochan Sahoo, Ron C Michaelis, et al.
Journal of Inherited Metabolic Disease
|
May 27, 2016
Erratum to: Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism
Marcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Elife
|
January 3, 2023
Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndrome
Dongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 27, 1999
Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons
N Morral, W O'Neal, K Rice, et al.
Elife
|
October 15, 2024
Correction: Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndrome
Dongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
BMC Biology
|
June 22, 2018
Comparative analysis of single-stranded DNA donors to generate conditional null mouse alleles
Denise G Lanza, Angelina Gaspero, Isabel Lorenzo, et al.
Journal of Inherited Metabolic Disease
|
April 16, 2015
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism
Marcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Prenatal Diagnosis
|
October 21, 2016
Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women
Steen Kølvraa, Ripudaman Singh, Elizabeth A Normand, et al.
Nature Genetics
|
November 10, 2009
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes
Marwan Shinawi, Christian P Schaaf, Samarth S Bhatt, et al.
Page
of 46
Search research articles
Search
Showing results (371-380 of 456) with videos related to
Sort By:
Page
of 46
Prenatal Diagnosis
|
February 27, 2024
Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical study
Michelle Bellair, Elisabete Amaral, Mason Ouren, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2004
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A
Yong-Hui Jiang, Trilochan Sahoo, Ron C Michaelis, et al.
Journal of Inherited Metabolic Disease
|
May 27, 2016
Erratum to: Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism
Marcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Elife
|
January 3, 2023
Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndrome
Dongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 27, 1999
Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons
N Morral, W O'Neal, K Rice, et al.
Elife
|
October 15, 2024
Correction: Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndrome
Dongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
BMC Biology
|
June 22, 2018
Comparative analysis of single-stranded DNA donors to generate conditional null mouse alleles
Denise G Lanza, Angelina Gaspero, Isabel Lorenzo, et al.
Journal of Inherited Metabolic Disease
|
April 16, 2015
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism
Marcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Prenatal Diagnosis
|
October 21, 2016
Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women
Steen Kølvraa, Ripudaman Singh, Elizabeth A Normand, et al.
Nature Genetics
|
November 10, 2009
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes
Marwan Shinawi, Christian P Schaaf, Samarth S Bhatt, et al.
Page
of 46