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Pediatric Research
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September 27, 2005
TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome
Deborah A McDermott, Michael C Bressan, Jie He, et al.
Journal of Medical Genetics
|
July 3, 2021
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects
Yoav Bolkier, Ortal Barel, Dina Marek-Yagel, et al.
Frontiers in Genetics
|
January 26, 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders
Maayan Kagan, Rotem Semo-Oz, Yishay Ben Moshe, et al.
American Journal of Medical Genetics. Part A
|
November 2, 2011
The male phenotype in osteopathia striata congenita with cranial sclerosis
Sarah K Holman, Phil Daniel, Zandra A Jenkins, et al.
Human Molecular Genetics
|
April 16, 2008
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity
Miriam Gordillo, Hugo Vega, Alison H Trainer, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2005
Further delineation of Kabuki syndrome in 48 well-defined new individuals
Linlea Armstrong, Azza Abd El Moneim, Kirk Aleck, et al.
American Journal of Human Genetics
|
November 8, 2016
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder
Gali Heimer, Juha M Kerätär, Lisa G Riley, et al.
Scientific Reports
|
September 28, 2021
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies
Ben Pode-Shakked, Ortal Barel, Amihood Singer, et al.
European Journal of Human Genetics : EJHG
|
January 16, 2014
Myhre and LAPS syndromes: clinical and molecular review of 32 patients
Caroline Michot, Carine Le Goff, Clémentine Mahaut, et al.
European Journal of Human Genetics : EJHG
|
February 19, 2021
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants
Sandra Whalen, Marie Shaw, Cyril Mignot, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 89) with videos related to
Sort By:
Page
of 9
Pediatric Research
|
September 27, 2005
TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome
Deborah A McDermott, Michael C Bressan, Jie He, et al.
Journal of Medical Genetics
|
July 3, 2021
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects
Yoav Bolkier, Ortal Barel, Dina Marek-Yagel, et al.
Frontiers in Genetics
|
January 26, 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders
Maayan Kagan, Rotem Semo-Oz, Yishay Ben Moshe, et al.
American Journal of Medical Genetics. Part A
|
November 2, 2011
The male phenotype in osteopathia striata congenita with cranial sclerosis
Sarah K Holman, Phil Daniel, Zandra A Jenkins, et al.
Human Molecular Genetics
|
April 16, 2008
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity
Miriam Gordillo, Hugo Vega, Alison H Trainer, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2005
Further delineation of Kabuki syndrome in 48 well-defined new individuals
Linlea Armstrong, Azza Abd El Moneim, Kirk Aleck, et al.
American Journal of Human Genetics
|
November 8, 2016
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder
Gali Heimer, Juha M Kerätär, Lisa G Riley, et al.
Scientific Reports
|
September 28, 2021
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies
Ben Pode-Shakked, Ortal Barel, Amihood Singer, et al.
European Journal of Human Genetics : EJHG
|
January 16, 2014
Myhre and LAPS syndromes: clinical and molecular review of 32 patients
Caroline Michot, Carine Le Goff, Clémentine Mahaut, et al.
European Journal of Human Genetics : EJHG
|
February 19, 2021
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants
Sandra Whalen, Marie Shaw, Cyril Mignot, et al.
Page
of 9