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Allen N Lamb

Showing results (1-10 of 29) with videos related to

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Clinics in Laboratory Medicine|November 29, 2011
Laboratory aspects of prenatal microarray analysisAllen N Lamb
Clinics in Laboratory Medicine|July 10, 2003
Cytogenetics and molecular cytogenetics in prenatal diagnosisAlan E Donnenfeld, Allen N Lamb
Expert Opinion on Medical Diagnostics|March 16, 2013
Detecting genomic imbalances in prenatal diagnosis: main hurdles and recent advancesSarah T South, Allen N Lamb
Molecular Cytogenetics|May 28, 2019
Clinical and molecular cytogenetic characterization of a novel 10q interstitial deletion: a case report and review of the literatureJohn C Herriges, Sarah L Dugan, Allen N Lamb
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2003
Prenatal diagnosis from fetal urine in bladder outlet obstruction: success rates for traditional cytogenetic evaluation and interphase fluorescence in situ hybridizationAlan E Donnenfeld, David Lockwood, Trace Custer, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disabilityErica F Andersen, Erin E Baldwin, Sara Ellingwood, et al.
European Journal of Medical Genetics|May 31, 2016
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorderGifty Bhat, Danielle LaGrave, Alison Millson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 28, 2013
ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013Sarah T South, Charles Lee, Allen N Lamb, et al.
Prenatal Diagnosis|October 2, 2009
Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarrayJustine Coppinger, Sarah Alliman, Allen N Lamb, et al.
Cytogenetic and Genome Research|September 6, 2019
A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental DelayPrabakaran Paulraj, Michelle Bosworth, Maria Longhurst, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Clinics in Laboratory Medicine|November 29, 2011
Laboratory aspects of prenatal microarray analysisAllen N Lamb
Clinics in Laboratory Medicine|July 10, 2003
Cytogenetics and molecular cytogenetics in prenatal diagnosisAlan E Donnenfeld, Allen N Lamb
Expert Opinion on Medical Diagnostics|March 16, 2013
Detecting genomic imbalances in prenatal diagnosis: main hurdles and recent advancesSarah T South, Allen N Lamb
Molecular Cytogenetics|May 28, 2019
Clinical and molecular cytogenetic characterization of a novel 10q interstitial deletion: a case report and review of the literatureJohn C Herriges, Sarah L Dugan, Allen N Lamb
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2003
Prenatal diagnosis from fetal urine in bladder outlet obstruction: success rates for traditional cytogenetic evaluation and interphase fluorescence in situ hybridizationAlan E Donnenfeld, David Lockwood, Trace Custer, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disabilityErica F Andersen, Erin E Baldwin, Sara Ellingwood, et al.
European Journal of Medical Genetics|May 31, 2016
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorderGifty Bhat, Danielle LaGrave, Alison Millson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 28, 2013
ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013Sarah T South, Charles Lee, Allen N Lamb, et al.
Prenatal Diagnosis|October 2, 2009
Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarrayJustine Coppinger, Sarah Alliman, Allen N Lamb, et al.
Cytogenetic and Genome Research|September 6, 2019
A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental DelayPrabakaran Paulraj, Michelle Bosworth, Maria Longhurst, et al.
Pageof 3