J E Ming|M Muenke - JoVE Visualize

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American Journal of Human Genetics|January 13, 2000

Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.

Revista De Neurologia|April 3, 2009

[Attention deficit hyperactivity behavioral phenotype dimensions of adults from Antioquian families using the Wender-Utah Scale -Spanish version]N Trujillo-Orrego, D A Pineda, C P Arango, et al.

Human Molecular Genetics|April 4, 2001

Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.

American Journal of Medical Genetics|December 26, 2001

Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrencesK L Russell, J E Ming, K Patel, et al.

American Journal of Medical Genetics|February 7, 1998

Heterotaxia in a fetus with campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys: expanding the phenotype of Cumming syndromeJ E Ming, D M McDonald-McGinn, R I Markowitz, et al.

Journal of Medical Genetics|October 4, 2005

Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.

Genes, Brain, and Behavior|November 3, 2010

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication studyM Ribasés, J A Ramos-Quiroga, C Sánchez-Mora, et al.

American Journal of Human Genetics|October 10, 2007

Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humansJ D Karkera, J S Lee, E Roessler, et al.

Molecular Psychiatry|November 25, 2015

Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolateC A Mastronardi, E Pillai, D A Pineda, et al.

Diabetes|June 28, 2000

Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing InvestigatorsC A Stanley, J Fang, K Kutyna, et al.

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Showing results (81-90 of 112) with videos related to

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American Journal of Human Genetics|January 13, 2000

Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.

Revista De Neurologia|April 3, 2009

[Attention deficit hyperactivity behavioral phenotype dimensions of adults from Antioquian families using the Wender-Utah Scale -Spanish version]N Trujillo-Orrego, D A Pineda, C P Arango, et al.

Human Molecular Genetics|April 4, 2001

Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.

American Journal of Medical Genetics|December 26, 2001

Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrencesK L Russell, J E Ming, K Patel, et al.

American Journal of Medical Genetics|February 7, 1998

Heterotaxia in a fetus with campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys: expanding the phenotype of Cumming syndromeJ E Ming, D M McDonald-McGinn, R I Markowitz, et al.

Journal of Medical Genetics|October 4, 2005

Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.

Genes, Brain, and Behavior|November 3, 2010

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication studyM Ribasés, J A Ramos-Quiroga, C Sánchez-Mora, et al.

American Journal of Human Genetics|October 10, 2007

Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humansJ D Karkera, J S Lee, E Roessler, et al.

Molecular Psychiatry|November 25, 2015

Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolateC A Mastronardi, E Pillai, D A Pineda, et al.

Diabetes|June 28, 2000

Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing InvestigatorsC A Stanley, J Fang, K Kutyna, et al.

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