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Pediatrics
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November 9, 2011
Cobalamin F disease detected by newborn screening and follow-up on a 14-year-old patient
Olajumoke Oladipo, David S Rosenblatt, David Watkins, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
May 21, 2009
The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations
Robin P Goin-Kochel, Anne E Porter, Sarika U Peters, et al.
American Journal of Medical Genetics. Part A
|
November 20, 2016
Neuroligin 2 nonsense variant associated with anxiety, autism, intellectual disability, hyperphagia, and obesity
Daniel J Parente, Caryn Garriga, Berivan Baskin, et al.
American Journal of Medical Genetics. Part A
|
November 26, 2015
Multigenerational autosomal dominant inheritance of 5p chromosomal deletions
Bin Zhang, Marcia Willing, Dorothy K Grange, et al.
Child Neurology Open
|
October 21, 2017
CEDNIK: Phenotypic and Molecular Characterization of an Additional Patient and Review of the Literature
Tina Hsu, Carrie C Coughlin, Kristin G Monaghan, et al.
American Journal of Medical Genetics. Part A
|
June 19, 2008
15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization
Nicola Brunetti-Pierri, Trilochan Sahoo, Sarah Frioux, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2012
Duplication of 20p12.3 associated with familial Wolff-Parkinson-White syndrome
Kimberly I Mills, Jacqueline Anderson, Philip T Levy, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome
Richard J Schroer, Arthur L Beaudet, Marwan Shinawi, et al.
Bone
|
March 28, 2019
Phenotype and response to growth hormone therapy in siblings with B4GALT7 deficiency
Carla Sandler-Wilson, Jennifer A Wambach, Bess A Marshall, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2008
Delineation of the proximal 3q microdeletion syndrome
Marcia J Simovich, Steven D Bland, Daniel A Peiffer, et al.
Page
of 17
Search research articles
Search
Showing results (51-60 of 170) with videos related to
Sort By:
Page
of 17
Pediatrics
|
November 9, 2011
Cobalamin F disease detected by newborn screening and follow-up on a 14-year-old patient
Olajumoke Oladipo, David S Rosenblatt, David Watkins, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
May 21, 2009
The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations
Robin P Goin-Kochel, Anne E Porter, Sarika U Peters, et al.
American Journal of Medical Genetics. Part A
|
November 20, 2016
Neuroligin 2 nonsense variant associated with anxiety, autism, intellectual disability, hyperphagia, and obesity
Daniel J Parente, Caryn Garriga, Berivan Baskin, et al.
American Journal of Medical Genetics. Part A
|
November 26, 2015
Multigenerational autosomal dominant inheritance of 5p chromosomal deletions
Bin Zhang, Marcia Willing, Dorothy K Grange, et al.
Child Neurology Open
|
October 21, 2017
CEDNIK: Phenotypic and Molecular Characterization of an Additional Patient and Review of the Literature
Tina Hsu, Carrie C Coughlin, Kristin G Monaghan, et al.
American Journal of Medical Genetics. Part A
|
June 19, 2008
15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization
Nicola Brunetti-Pierri, Trilochan Sahoo, Sarah Frioux, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2012
Duplication of 20p12.3 associated with familial Wolff-Parkinson-White syndrome
Kimberly I Mills, Jacqueline Anderson, Philip T Levy, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome
Richard J Schroer, Arthur L Beaudet, Marwan Shinawi, et al.
Bone
|
March 28, 2019
Phenotype and response to growth hormone therapy in siblings with B4GALT7 deficiency
Carla Sandler-Wilson, Jennifer A Wambach, Bess A Marshall, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2008
Delineation of the proximal 3q microdeletion syndrome
Marcia J Simovich, Steven D Bland, Daniel A Peiffer, et al.
Page
of 17