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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 17, 2015
Recognition and prevention of child abuse in the child with disability
Catherine Bearce Nowak
Seminars in Pediatric Neurology
|
November 6, 2007
The phakomatoses: dermatologic clues to neurologic anomalies
Catherine Bearce Nowak
American Journal of Medical Genetics. Part A
|
May 6, 2016
In memory of Murray Feingold (1930-2015)
G Bradley Schaefer, Catherine Bearce Nowak, Ann Haskins Olney
American Journal of Medical Genetics. Part A
|
June 9, 2016
Is one diagnosis the whole story? patients with double diagnoses
Alina Kurolap, Naama Orenstein, Inbal Kedar, et al.
Human Mutation
|
June 1, 2018
Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery
Raman Kumar, Alison Gardner, Claire C Homan, et al.
European Journal of Human Genetics : EJHG
|
July 26, 2024
Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals
Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree, et al.
European Journal of Human Genetics : EJHG
|
April 27, 2024
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals
Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 17, 2015
Recognition and prevention of child abuse in the child with disability
Catherine Bearce Nowak
Seminars in Pediatric Neurology
|
November 6, 2007
The phakomatoses: dermatologic clues to neurologic anomalies
Catherine Bearce Nowak
American Journal of Medical Genetics. Part A
|
May 6, 2016
In memory of Murray Feingold (1930-2015)
G Bradley Schaefer, Catherine Bearce Nowak, Ann Haskins Olney
American Journal of Medical Genetics. Part A
|
June 9, 2016
Is one diagnosis the whole story? patients with double diagnoses
Alina Kurolap, Naama Orenstein, Inbal Kedar, et al.
Human Mutation
|
June 1, 2018
Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery
Raman Kumar, Alison Gardner, Claire C Homan, et al.
European Journal of Human Genetics : EJHG
|
July 26, 2024
Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals
Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree, et al.
European Journal of Human Genetics : EJHG
|
April 27, 2024
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals
Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree, et al.
Page
of 1