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Nancy B Spinner

Showing results (61-70 of 140) with videos related to

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American Journal of Medical Genetics. Part A|April 11, 2012
Alagille syndrome in a Vietnamese cohort: mutation analysis and assessment of facial featuresHenry C Lin, Phuc Le Hoang, Anne Hutchinson, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung diseaseMatthew G Sampson, Curtis R Coughlin, Paige Kaplan, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 2, 2005
Intracranial vascular abnormalities in patients with Alagille syndromeKaran M Emerick, Ian D Krantz, Binita M Kamath, et al.
Journal of Applied Genetics|April 22, 2014
Spectrum of JAG1 gene mutations in Polish patients with Alagille syndromeDorota Jurkiewicz, Dorota Gliwicz, Elżbieta Ciara, et al.
The Journal of Pediatrics|December 4, 2014
Moyamoya syndrome associated with Alagille syndrome: outcome after surgical revascularizationLissa C Baird, Edward R Smith, Rebecca Ichord, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 7, 2002
Rep/Cap gene amplification and high-yield production of AAV in an A549 cell line expressing Rep/CapGuang-ping Gao, Fengmin Lu, Julio C Sanmiguel, et al.
Human Mutation|March 14, 2015
Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresiaEllen A Tsai, Christopher M Grochowski, Alexandra M Falsey, et al.
American Journal of Medical Genetics|September 24, 2002
Facial features in Alagille syndrome: specific or cholestasis facies?Binita M Kamath, Kathleen M Loomes, Rebecca J Oakey, et al.
American Journal of Medical Genetics. Part A|October 15, 2011
Mosaic trisomy 17: variable clinical and cytogenetic presentationRobert Daber, Kimberly A Chapman, Eduardo Ruchelli, et al.
American Journal of Medical Genetics. Part A|May 16, 2017
CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issuesMinjie Luo, Jinbo Fan, Tara L Wenger, et al.
Pageof 14

Showing results (61-70 of 140) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part A|April 11, 2012
Alagille syndrome in a Vietnamese cohort: mutation analysis and assessment of facial featuresHenry C Lin, Phuc Le Hoang, Anne Hutchinson, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung diseaseMatthew G Sampson, Curtis R Coughlin, Paige Kaplan, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 2, 2005
Intracranial vascular abnormalities in patients with Alagille syndromeKaran M Emerick, Ian D Krantz, Binita M Kamath, et al.
Journal of Applied Genetics|April 22, 2014
Spectrum of JAG1 gene mutations in Polish patients with Alagille syndromeDorota Jurkiewicz, Dorota Gliwicz, Elżbieta Ciara, et al.
The Journal of Pediatrics|December 4, 2014
Moyamoya syndrome associated with Alagille syndrome: outcome after surgical revascularizationLissa C Baird, Edward R Smith, Rebecca Ichord, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 7, 2002
Rep/Cap gene amplification and high-yield production of AAV in an A549 cell line expressing Rep/CapGuang-ping Gao, Fengmin Lu, Julio C Sanmiguel, et al.
Human Mutation|March 14, 2015
Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresiaEllen A Tsai, Christopher M Grochowski, Alexandra M Falsey, et al.
American Journal of Medical Genetics|September 24, 2002
Facial features in Alagille syndrome: specific or cholestasis facies?Binita M Kamath, Kathleen M Loomes, Rebecca J Oakey, et al.
American Journal of Medical Genetics. Part A|October 15, 2011
Mosaic trisomy 17: variable clinical and cytogenetic presentationRobert Daber, Kimberly A Chapman, Eduardo Ruchelli, et al.
American Journal of Medical Genetics. Part A|May 16, 2017
CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issuesMinjie Luo, Jinbo Fan, Tara L Wenger, et al.
Pageof 14