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Journal of Pediatric Gastroenterology and Nutrition
|
August 2, 2007
Gastric rupture and necrosis in Prader-Willi syndrome
David A Stevenson, Janalee Heinemann, Moris Angulo, et al.
International Journal of Molecular Sciences
|
August 27, 2021
Arteriovenous Malformations-Current Understanding of the Pathogenesis with Implications for Treatment
Katharina Schimmel, Md Khadem Ali, Serena Y Tan, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2016
Respiratory system involvement in Costello syndrome
Natalia Gomez-Ospina, Christin Kuo, Amitha Lakshmi Ananth, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 19, 2008
Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement
David A Stevenson, John C Carey, Stephen P Coburn, et al.
The Journal of Pediatrics
|
December 26, 2006
Bone mineral density in children and adolescents with neurofibromatosis type 1
David A Stevenson, Laurie J Moyer-Mileur, Mary Murray, et al.
Plos One
|
July 21, 2015
Genetic Variants Associated with Port-Wine Stains
Alice Frigerio, Karol Wright, Whitney Wooderchak-Donahue, et al.
The Journal of Molecular Diagnostics : JMD
|
April 24, 2017
Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis
Rebecca L Margraf, Chad VanSant-Webb, David Sant, et al.
American Journal of Medical Genetics. Part A
|
September 7, 2023
Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome
Ryan W Gates, Bryn D Webb, David A Stevenson, et al.
American Journal of Medical Genetics. Part A
|
April 11, 2026
CBL Syndrome With Granular Cell Tumor and café au lait macules: Expansion of the Phenotype
Caitlin N Harrington, Emily Kohl, Zainab Gilitwala, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2006
Deaths due to choking in Prader-Willi syndrome
David A Stevenson, Janalee Heinemann, Moris Angulo, et al.
Page
of 17
Search research articles
Search
Showing results (71-80 of 166) with videos related to
Sort By:
Page
of 17
Journal of Pediatric Gastroenterology and Nutrition
|
August 2, 2007
Gastric rupture and necrosis in Prader-Willi syndrome
David A Stevenson, Janalee Heinemann, Moris Angulo, et al.
International Journal of Molecular Sciences
|
August 27, 2021
Arteriovenous Malformations-Current Understanding of the Pathogenesis with Implications for Treatment
Katharina Schimmel, Md Khadem Ali, Serena Y Tan, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2016
Respiratory system involvement in Costello syndrome
Natalia Gomez-Ospina, Christin Kuo, Amitha Lakshmi Ananth, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 19, 2008
Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement
David A Stevenson, John C Carey, Stephen P Coburn, et al.
The Journal of Pediatrics
|
December 26, 2006
Bone mineral density in children and adolescents with neurofibromatosis type 1
David A Stevenson, Laurie J Moyer-Mileur, Mary Murray, et al.
Plos One
|
July 21, 2015
Genetic Variants Associated with Port-Wine Stains
Alice Frigerio, Karol Wright, Whitney Wooderchak-Donahue, et al.
The Journal of Molecular Diagnostics : JMD
|
April 24, 2017
Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis
Rebecca L Margraf, Chad VanSant-Webb, David Sant, et al.
American Journal of Medical Genetics. Part A
|
September 7, 2023
Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome
Ryan W Gates, Bryn D Webb, David A Stevenson, et al.
American Journal of Medical Genetics. Part A
|
April 11, 2026
CBL Syndrome With Granular Cell Tumor and café au lait macules: Expansion of the Phenotype
Caitlin N Harrington, Emily Kohl, Zainab Gilitwala, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2006
Deaths due to choking in Prader-Willi syndrome
David A Stevenson, Janalee Heinemann, Moris Angulo, et al.
Page
of 17