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Journal of Child Neurology
|
November 26, 2004
Molecular genetic basis of tuberous sclerosis complex: from bench to bedside
Kit-Sing Au, Aimee T Williams, Michael J Gambello, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 17, 2006
Tuberous sclerosis complex and polycystic kidney disease together: an exception to the contiguous gene syndrome
Audrey C Woerner, Kit-Sing Au, Aimee T Williams, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
September 14, 2016
Genetic association of the glycine cleavage system genes and myelomeningocele
Rita H Shah, Hope Northrup, James E Hixson, et al.
Development (Cambridge, England)
|
November 20, 2020
<i>Snx3</i> is important for mammalian neural tube closure via its role in canonical and non-canonical WNT signaling
Heather Mary Brown, Stephen A Murray, Hope Northrup, et al.
Clinical Endocrinology
|
November 6, 2010
Mutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets
Mary D Ruppe, Patrick G Brosnan, Kit Sing Au, et al.
Birth Defects Research
|
July 8, 2016
Maternal gene-micronutrient interactions related to one-carbon metabolism and the risk of myelomeningocele among offspring
Margaret P Nguyen, Philip J Lupo, Hope Northrup, et al.
BMC Medical Education
|
November 24, 2020
Association between training experience and readiness for advance care planning among healthcare professionals: a cross-sectional study
Helen Yue-Lai Chan, Annie Oi-Ling Kwok, Kwok-Keung Yuen, et al.
Reproductive Sciences (Thousand Oaks, Calif.)
|
January 24, 2008
Genes in glucose metabolism and association with spina bifida
Christina M Davidson, Hope Northrup, Terri M King, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
January 22, 2011
Association of retinoic acid receptor genes with meningomyelocele
Phong X Tran, Kit Sing Au, Alanna C Morrison, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2017
Mutations in folate transporter genes and risk for human myelomeningocele
Tina O Findley, Joy C Tenpenny, Michelle R O'Byrne, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 53) with videos related to
Sort By:
Page
of 6
Journal of Child Neurology
|
November 26, 2004
Molecular genetic basis of tuberous sclerosis complex: from bench to bedside
Kit-Sing Au, Aimee T Williams, Michael J Gambello, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 17, 2006
Tuberous sclerosis complex and polycystic kidney disease together: an exception to the contiguous gene syndrome
Audrey C Woerner, Kit-Sing Au, Aimee T Williams, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
September 14, 2016
Genetic association of the glycine cleavage system genes and myelomeningocele
Rita H Shah, Hope Northrup, James E Hixson, et al.
Development (Cambridge, England)
|
November 20, 2020
<i>Snx3</i> is important for mammalian neural tube closure via its role in canonical and non-canonical WNT signaling
Heather Mary Brown, Stephen A Murray, Hope Northrup, et al.
Clinical Endocrinology
|
November 6, 2010
Mutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets
Mary D Ruppe, Patrick G Brosnan, Kit Sing Au, et al.
Birth Defects Research
|
July 8, 2016
Maternal gene-micronutrient interactions related to one-carbon metabolism and the risk of myelomeningocele among offspring
Margaret P Nguyen, Philip J Lupo, Hope Northrup, et al.
BMC Medical Education
|
November 24, 2020
Association between training experience and readiness for advance care planning among healthcare professionals: a cross-sectional study
Helen Yue-Lai Chan, Annie Oi-Ling Kwok, Kwok-Keung Yuen, et al.
Reproductive Sciences (Thousand Oaks, Calif.)
|
January 24, 2008
Genes in glucose metabolism and association with spina bifida
Christina M Davidson, Hope Northrup, Terri M King, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
January 22, 2011
Association of retinoic acid receptor genes with meningomyelocele
Phong X Tran, Kit Sing Au, Alanna C Morrison, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2017
Mutations in folate transporter genes and risk for human myelomeningocele
Tina O Findley, Joy C Tenpenny, Michelle R O'Byrne, et al.
Page
of 6