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Nancy B Spinner

Showing results (31-40 of 140) with videos related to

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American Journal of Medical Genetics. Part A|November 9, 2011
8p21 microdeletion in a patient with intellectual disability and behavioral abnormalitiesKosuke Izumi, Heather Mikesell, Robert Daber, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2012
"What does it mean?": uncertainties in understanding results of chromosomal microarray testingMarian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, et al.
Journal of Autism and Developmental Disorders|February 24, 2017
"Set in Stone" or "Ray of Hope": Parents' Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASDMarian Reiff, Eva Bugos, Ellen Giarelli, et al.
Journal of Autism and Developmental Disorders|June 13, 2015
Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disordersMarian Reiff, Ellen Giarelli, Barbara A Bernhardt, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 28, 2010
A longitudinal study to identify laboratory predictors of liver disease outcome in Alagille syndromeBinita M Kamath, Pedro S Munoz, Natalie Bab, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypesEmma A Schindler, Melissa A Gilbert, David A Piccoli, et al.
American Journal of Medical Genetics|September 24, 2002
Alagille syndrome inherited from a phenotypically normal mother with a mosaic 20p microdeletionAyala Laufer-Cahana, Ian D Krantz, Lynn D Bason, et al.
American Journal of Medical Genetics. Part A|August 3, 2005
Chromosome rearrangements in cornelia de Lange syndrome (CdLS): report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangementsCheryl DeScipio, Maninder Kaur, Dinah Yaeger, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 6, 2010
Effect of Kasai procedure on hepatic outcome in Alagille syndromeAdam J Kaye, Elizabeth B Rand, Pedro S Munoz, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septumMoira A Crowley, Laura K Conlin, Elaine H Zackai, et al.
Pageof 14

Showing results (31-40 of 140) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part A|November 9, 2011
8p21 microdeletion in a patient with intellectual disability and behavioral abnormalitiesKosuke Izumi, Heather Mikesell, Robert Daber, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2012
"What does it mean?": uncertainties in understanding results of chromosomal microarray testingMarian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, et al.
Journal of Autism and Developmental Disorders|February 24, 2017
"Set in Stone" or "Ray of Hope": Parents' Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASDMarian Reiff, Eva Bugos, Ellen Giarelli, et al.
Journal of Autism and Developmental Disorders|June 13, 2015
Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disordersMarian Reiff, Ellen Giarelli, Barbara A Bernhardt, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 28, 2010
A longitudinal study to identify laboratory predictors of liver disease outcome in Alagille syndromeBinita M Kamath, Pedro S Munoz, Natalie Bab, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypesEmma A Schindler, Melissa A Gilbert, David A Piccoli, et al.
American Journal of Medical Genetics|September 24, 2002
Alagille syndrome inherited from a phenotypically normal mother with a mosaic 20p microdeletionAyala Laufer-Cahana, Ian D Krantz, Lynn D Bason, et al.
American Journal of Medical Genetics. Part A|August 3, 2005
Chromosome rearrangements in cornelia de Lange syndrome (CdLS): report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangementsCheryl DeScipio, Maninder Kaur, Dinah Yaeger, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 6, 2010
Effect of Kasai procedure on hepatic outcome in Alagille syndromeAdam J Kaye, Elizabeth B Rand, Pedro S Munoz, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septumMoira A Crowley, Laura K Conlin, Elaine H Zackai, et al.
Pageof 14