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Golder N Wilson

Showing results (11-20 of 32) with videos related to

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American Journal of Medical Genetics. Part A|February 25, 2003
Coming together for blastogenesisGolder N Wilson
Archives of Neurology|November 10, 2004
Tales from the neural genome: the lessons of homozygous porphyriaGolder N Wilson
American Journal of Medical Genetics. Part A|July 4, 2015
Registry analysis supports different mechanisms for gastroschisis and omphalocele within shared developmental fieldsBonna Benjamin, Golder N Wilson
American Journal of Medical Genetics. Part A|April 4, 2003
Behavioral assessment of children with Down syndrome using the Reiss psychopathology scaleDebbie Clark, Golder N Wilson
Journal of Pediatric Surgery|April 15, 2014
Anomalies associated with gastroschisis and omphalocele: analysis of 2825 cases from the Texas Birth Defects RegistryBonna Benjamin, Golder N Wilson
Current Issues in Molecular Biology|March 27, 2024
Clinical-Genomic Analysis of 1261 Patients with Ehlers-Danlos Syndrome Outlines an Articulo-Autonomic Gene Network (Entome)Golder N Wilson, Vijay S Tonk
American Journal of Medical Genetics. Part A|December 29, 2015
Inaccuracy of non-invasive prenatal screening demands cautious counsel and follow-upVijay S Tonk, Golder N Wilson
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 30, 2003
Biochemical abnormality associated with Smith-Lemli-Opitz syndrome in an infant with features of Rutledge multiple congenital anomaly syndrome confirms that the latter is a variant of the formerDinesh Rakheja, Golder N Wilson, Beverly B Rogers
American Journal of Medical Genetics. Part A|June 17, 2009
Al-Awadi/Raas-Rothschild/Schinzel (AARRS) phocomelia syndrome: case report and developmental field analysisMuhammad Subhani, Gangaram Akangire, Archana Kulkarni, et al.
Journal of Pediatric and Adolescent Gynecology|December 8, 2015
Chromosome Xq13.2 Microduplication Involving an X-Inactivation Gene in a Girl with Short Stature, Madelung Deformity, and von Willebrand DiseaseMarcela M Nur, Merick Yamada, Vijay Tonk, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part A|February 25, 2003
Coming together for blastogenesisGolder N Wilson
Archives of Neurology|November 10, 2004
Tales from the neural genome: the lessons of homozygous porphyriaGolder N Wilson
American Journal of Medical Genetics. Part A|July 4, 2015
Registry analysis supports different mechanisms for gastroschisis and omphalocele within shared developmental fieldsBonna Benjamin, Golder N Wilson
American Journal of Medical Genetics. Part A|April 4, 2003
Behavioral assessment of children with Down syndrome using the Reiss psychopathology scaleDebbie Clark, Golder N Wilson
Journal of Pediatric Surgery|April 15, 2014
Anomalies associated with gastroschisis and omphalocele: analysis of 2825 cases from the Texas Birth Defects RegistryBonna Benjamin, Golder N Wilson
Current Issues in Molecular Biology|March 27, 2024
Clinical-Genomic Analysis of 1261 Patients with Ehlers-Danlos Syndrome Outlines an Articulo-Autonomic Gene Network (Entome)Golder N Wilson, Vijay S Tonk
American Journal of Medical Genetics. Part A|December 29, 2015
Inaccuracy of non-invasive prenatal screening demands cautious counsel and follow-upVijay S Tonk, Golder N Wilson
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 30, 2003
Biochemical abnormality associated with Smith-Lemli-Opitz syndrome in an infant with features of Rutledge multiple congenital anomaly syndrome confirms that the latter is a variant of the formerDinesh Rakheja, Golder N Wilson, Beverly B Rogers
American Journal of Medical Genetics. Part A|June 17, 2009
Al-Awadi/Raas-Rothschild/Schinzel (AARRS) phocomelia syndrome: case report and developmental field analysisMuhammad Subhani, Gangaram Akangire, Archana Kulkarni, et al.
Journal of Pediatric and Adolescent Gynecology|December 8, 2015
Chromosome Xq13.2 Microduplication Involving an X-Inactivation Gene in a Girl with Short Stature, Madelung Deformity, and von Willebrand DiseaseMarcela M Nur, Merick Yamada, Vijay Tonk, et al.
Pageof 4