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Ted Brown

Showing results (321-330 of 330) with videos related to

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American Journal of Medical Genetics. Part A|February 28, 2013
Fragile X AGG analysis provides new risk predictions for 45-69 repeat allelesSarah L Nolin, Sachin Sah, Anne Glicksman, et al.
Journal of Medical Entomology|June 6, 2007
Human plague in the southwestern United States, 1957-2004: spatial models of elevated risk of human exposure to Yersinia pestisRebecca J Eisen, Russell E Enscore, Brad J Biggerstaff, et al.
Acta Neuropathologica|March 4, 2010
The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changesJerzy Wegiel, Izabela Kuchna, Krzysztof Nowicki, et al.
Human Mutation|July 15, 2015
POLD1 Germline Mutations in Patients Initially Diagnosed with Werner SyndromeDavor Lessel, Fuki M Hisama, Katalin Szakszon, et al.
Nature|April 26, 2003
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndromeMaria Eriksson, W Ted Brown, Leslie B Gordon, et al.
Journal of Neuropathology and Experimental Neurology|April 11, 2012
Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autismJerzy Wegiel, N Carolyn Schanen, Edwin H Cook, et al.
Brain Sciences|October 3, 2020
A Genotype-Phenotype Study of High-Resolution <i>FMR1</i> Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral AssessmentsDejan B Budimirovic, Annette Schlageter, Stela Filipovic-Sadic, et al.
American Journal of Human Genetics|January 17, 2003
Expansion of the fragile X CGG repeat in females with premutation or intermediate allelesSarah L Nolin, W Ted Brown, Anne Glicksman, et al.
Plos One|May 9, 2012
Abnormal intracellular accumulation and extracellular Aβ deposition in idiopathic and Dup15q11.2-q13 autism spectrum disordersJerzy Wegiel, Janusz Frackowiak, Bozena Mazur-Kolecka, et al.
Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.
Pageof 33

Showing results (321-330 of 330) with videos related to

Sort By:
Pageof 33
You have reached the last page of results.This site can display upto 330 results.
American Journal of Medical Genetics. Part A|February 28, 2013
Fragile X AGG analysis provides new risk predictions for 45-69 repeat allelesSarah L Nolin, Sachin Sah, Anne Glicksman, et al.
Journal of Medical Entomology|June 6, 2007
Human plague in the southwestern United States, 1957-2004: spatial models of elevated risk of human exposure to Yersinia pestisRebecca J Eisen, Russell E Enscore, Brad J Biggerstaff, et al.
Acta Neuropathologica|March 4, 2010
The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changesJerzy Wegiel, Izabela Kuchna, Krzysztof Nowicki, et al.
Human Mutation|July 15, 2015
POLD1 Germline Mutations in Patients Initially Diagnosed with Werner SyndromeDavor Lessel, Fuki M Hisama, Katalin Szakszon, et al.
Nature|April 26, 2003
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndromeMaria Eriksson, W Ted Brown, Leslie B Gordon, et al.
Journal of Neuropathology and Experimental Neurology|April 11, 2012
Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autismJerzy Wegiel, N Carolyn Schanen, Edwin H Cook, et al.
Brain Sciences|October 3, 2020
A Genotype-Phenotype Study of High-Resolution <i>FMR1</i> Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral AssessmentsDejan B Budimirovic, Annette Schlageter, Stela Filipovic-Sadic, et al.
American Journal of Human Genetics|January 17, 2003
Expansion of the fragile X CGG repeat in females with premutation or intermediate allelesSarah L Nolin, W Ted Brown, Anne Glicksman, et al.
Plos One|May 9, 2012
Abnormal intracellular accumulation and extracellular Aβ deposition in idiopathic and Dup15q11.2-q13 autism spectrum disordersJerzy Wegiel, Janusz Frackowiak, Bozena Mazur-Kolecka, et al.
Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.
Pageof 33