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American Journal of Medical Genetics. Part A
|
August 12, 2005
Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program
Barbara R Pober, Angela Lin, Meaghan Russell, et al.
Hypertension (Dallas, Tex. : 1979)
|
October 16, 2013
Williams syndrome predisposes to vascular stiffness modified by antihypertensive use and copy number changes in NCF1
Beth A Kozel, Joshua R Danback, Jessica L Waxler, et al.
Pediatric Cardiology
|
April 2, 2022
Frequency of QTc Interval Prolongation in Children and Adults with Williams Syndrome
Benjamin D Brink, Richard Feinn, Beth A Kozel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 9, 2012
Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes
Meaghan K Russell, Mauro Longoni, Julie Wells, et al.
American Journal of Medical Genetics. Part A
|
June 17, 2008
Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy
Sibel Kantarci, Nicola K Ragge, N Simon Thomas, et al.
Plos Genetics
|
August 17, 2005
Fog2 is required for normal diaphragm and lung development in mice and humans
Kate G Ackerman, Bruce J Herron, Sara O Vargas, et al.
American Journal of Medical Genetics. Part A
|
August 28, 2010
Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH
Sibel Kantarci, Kate G Ackerman, Meaghan K Russell, et al.
Journal of Autism and Developmental Disorders
|
February 18, 2016
Attention Bias to Emotional Faces Varies by IQ and Anxiety in Williams Syndrome
Lauren M McGrath, Joyce M Oates, Yael G Dai, et al.
The Journal of Pediatrics
|
August 31, 2016
Hypercalcemia in Patients with Williams-Beuren Syndrome
Sampat Sindhar, Michael Lugo, Mark D Levin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 27, 2008
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
Angela E Lin, Craig T Basson, Elizabeth Goldmuntz, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 57) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics. Part A
|
August 12, 2005
Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program
Barbara R Pober, Angela Lin, Meaghan Russell, et al.
Hypertension (Dallas, Tex. : 1979)
|
October 16, 2013
Williams syndrome predisposes to vascular stiffness modified by antihypertensive use and copy number changes in NCF1
Beth A Kozel, Joshua R Danback, Jessica L Waxler, et al.
Pediatric Cardiology
|
April 2, 2022
Frequency of QTc Interval Prolongation in Children and Adults with Williams Syndrome
Benjamin D Brink, Richard Feinn, Beth A Kozel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 9, 2012
Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes
Meaghan K Russell, Mauro Longoni, Julie Wells, et al.
American Journal of Medical Genetics. Part A
|
June 17, 2008
Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy
Sibel Kantarci, Nicola K Ragge, N Simon Thomas, et al.
Plos Genetics
|
August 17, 2005
Fog2 is required for normal diaphragm and lung development in mice and humans
Kate G Ackerman, Bruce J Herron, Sara O Vargas, et al.
American Journal of Medical Genetics. Part A
|
August 28, 2010
Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH
Sibel Kantarci, Kate G Ackerman, Meaghan K Russell, et al.
Journal of Autism and Developmental Disorders
|
February 18, 2016
Attention Bias to Emotional Faces Varies by IQ and Anxiety in Williams Syndrome
Lauren M McGrath, Joyce M Oates, Yael G Dai, et al.
The Journal of Pediatrics
|
August 31, 2016
Hypercalcemia in Patients with Williams-Beuren Syndrome
Sampat Sindhar, Michael Lugo, Mark D Levin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 27, 2008
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
Angela E Lin, Craig T Basson, Elizabeth Goldmuntz, et al.
Page
of 6