Molecular Cytogenetic Analysis of Telomere Rearrangements

Por Martin, Christa Lese, Ledbetter, David H.
Publicado no Curr Protoc Hum Genet (2015)

Genomic Variation: Lessons Learned from Whole-Genome CNV Analysis

Por Riggs, Erin Rooney, Ledbetter, David H., Martin, Christa Lese
Publicado em 2014

CNVs, Aneuploidies and Human Disease

Por Martin, Christa L., Kirkpatrick, Brianne E., Ledbetter, David H.
Publicado no Clin Perinatol (2015)

Genomic insights into the etiology and classification of the cerebral palsies

Por Moreno-De-Luca, Andres, Ledbetter, David H., Martin, Christa L.
Publicado em 2012

Shift happens: family background influences clinical variability in genetic neurodevelopmental disorders

Por Finucane, Brenda, Challman, Thomas D., Martin, Christa Lese, Ledbetter, David H.
Publicado no Genet Med (2016)

Characterization of Physical Gap Sizes at Human Telomeres

Por Lese, Christa M., Fantes, Judy A., Riethman, Harold C., Ledbetter, David H.
Publicado em 1999

The Human Aminophospholipid-Transporting ATPase Gene ATP10C Maps Adjacent to UBE3A and Exhibits Similar Imprinted Expression

Por Herzing, Laura B. K., Kim, Soo-Jeong, Cook, Jr., Edwin H., Ledbetter, David H.
Publicado em 2001

A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders

Por Gonzalez-Mantilla, Andrea J., Moreno-De-Luca, Andres, Ledbetter, David H., Martin, Christa Lese
Publicado no JAMA Psychiatry (2016)

The Evolutionary Origin of Human Subtelomeric Homologies—or Where the Ends Begin

Por Martin, Christa Lese, Wong, Andrew, Gross, Alyssa, Chung, June, Fantes, Judy A., Ledbetter, David H.
Publicado em 2002

Comparative Genomic Hybridization–Array Analysis Enhances the Detection of Aneuploidies and Submicroscopic Imbalances in Spontaneous Miscarriages

Por Schaeffer, Anthony J. , Chung, June , Heretis, Konstantina , Wong, Andrew , Ledbetter, David H. , Lese Martin, Christa 
Publicado em 2004

Mechanisms and Consequences of Small Supernumerary Marker Chromosomes: From Barbara McClintock to Modern Genetic-Counseling Issues

Por Baldwin, Erin L., May, Lorraine F., Justice, April N., Martin, Christa L., Ledbetter, David H.
Publicado em 2008

Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci

Por Weber, James L., Kwitek, Anne E., May, Paula E., Wallace, Margaret R., Collins, Francis S., Ledbetter, David H.
Publicado em 1990

American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy

Por Shaffer, Lisa G., Agan, Noelle, Goldberg, James D., Ledbetter, David H., Longshore, John W., Cassidy, Suzanne B.
Publicado em 2001

Genomic Organization of the Murine Miller–Dieker/Lissencephaly Region: Conservation of Linkage with the Human Region

Por Hirotsune, Shinji, Pack, Svetlana D., Chong, Samuel S., Robbins, Christiane M., Pavan, William J., Ledbetter, David H., Wynshaw-Boris, Anthony
Publicado em 1997

Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence

Por Moreno-De-Luca, Andres, Myers, Scott M., Challman, Thomas D., Moreno-De-Luca, Daniel, Evans, David W., Ledbetter, David H.
Publicado em 2013

Human Preferences for Symmetry: Subjective Experience, Cognitive Conflict and Cortical Brain Activity

Por Evans, David W., Orr, Patrick T., Lazar, Steven M., Breton, Daniel, Gerard, Jennifer, Ledbetter, David H., Janosco, Kathleen, Dotts, Jessica, Batchelder, Holly
Publicado em 2012

Segmental duplications mediate novel, clinically relevant chromosome rearrangements

Por Rudd, M. Katharine, Keene, Julia, Bunke, Brian, Kaminsky, Erin B., Adam, Margaret P., Mulle, Jennifer G., Ledbetter, David H., Martin, Christa L.
Publicado em 2009

AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)

Por Cacciagli, Pierre, Desvignes, Jean-Pierre, Girard, Nadine, Delepine, Marc, Zelenika, Diana, Lathrop, Mark, Lévy, Nicolas, Ledbetter, David H, Dobyns, William B, Villard, Laurent
Publicado em 2014

GenomeConnect: matchmaking between patients, clinical laboratories and researchers to improve genomic knowledge

Por Kirkpatrick, Brianne E., Riggs, Erin Rooney, Azzariti, Danielle R., Miller, Vanessa Rangel, Ledbetter, David H., Miller, David T., Rehm, Heidi, Martin, Christa Lese, Faucett, W. Andrew
Publicado no Hum Mutat (2015)

Integrated YAC Contig Map of the Prader–Willi/Angelman Region on Chromosome 15q11–q13 with Average STS Spacing of 35 kb

Por Christian, Susan L., Bhatt, Nehal K., Martin, Scott A., Sutcliffe, James S., Kubota, Takeo, Huang, Bing, Mutirangura, Apiwat, Chinault, A. Craig, Beaudet, Arthur L., Ledbetter, David H.
Publicado em 1998