Search research articles
Contact Us
Filters
Showing results (11-20 of 95) with videos related to
Page
of 10
Sort By:
Clinics in Perinatology
|
June 5, 2015
Copy number variants, aneuploidies, and human disease
Christa Lese Martin, Brianne E Kirkpatrick, David H Ledbetter
Prenatal Diagnosis
|
November 19, 2016
Prognostic dilemmas and genetic counseling for prenatally detected fragile X gene expansions
Brenda Finucane, Sharyn Lincoln, Lindsay Bailey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 10, 2015
Shift happens: family background influences clinical variability in genetic neurodevelopmental disorders
Brenda Finucane, Thomas D Challman, Christa Lese Martin, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2004
Mitotic and meiotic instability of a telomere association involving the Y chromosome
Bing Huang, Christa Lese Martin, Constance J Sandlin, et al.
JAMA Psychiatry
|
January 29, 2016
A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders
Andrea J Gonzalez-Mantilla, Andres Moreno-De-Luca, David H Ledbetter, et al.
European Journal of Human Genetics : EJHG
|
June 21, 2007
3rd International Meeting on Cryptic Chromosomal Rearrangements in Mental Retardation and Autism
Corrado Romano, Samantha J L Knight, Christa Lese Martin, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
April 23, 2023
Letter to the editor
Brenda Finucane, Scott M Myers, Thomas D Challman, et al.
American Journal of Human Genetics
|
May 6, 2004
Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages
Anthony J Schaeffer, June Chung, Konstantina Heretis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 22, 2008
Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p
Xueya Hauge, Gordana Raca, Sara Cooper, et al.
American Journal of Human Genetics
|
March 5, 2002
The evolutionary origin of human subtelomeric homologies--or where the ends begin
Christa Lese Martin, Andrew Wong, Alyssa Gross, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 95) with videos related to
Sort By:
Page
of 10
Clinics in Perinatology
|
June 5, 2015
Copy number variants, aneuploidies, and human disease
Christa Lese Martin, Brianne E Kirkpatrick, David H Ledbetter
Prenatal Diagnosis
|
November 19, 2016
Prognostic dilemmas and genetic counseling for prenatally detected fragile X gene expansions
Brenda Finucane, Sharyn Lincoln, Lindsay Bailey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 10, 2015
Shift happens: family background influences clinical variability in genetic neurodevelopmental disorders
Brenda Finucane, Thomas D Challman, Christa Lese Martin, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2004
Mitotic and meiotic instability of a telomere association involving the Y chromosome
Bing Huang, Christa Lese Martin, Constance J Sandlin, et al.
JAMA Psychiatry
|
January 29, 2016
A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders
Andrea J Gonzalez-Mantilla, Andres Moreno-De-Luca, David H Ledbetter, et al.
European Journal of Human Genetics : EJHG
|
June 21, 2007
3rd International Meeting on Cryptic Chromosomal Rearrangements in Mental Retardation and Autism
Corrado Romano, Samantha J L Knight, Christa Lese Martin, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
April 23, 2023
Letter to the editor
Brenda Finucane, Scott M Myers, Thomas D Challman, et al.
American Journal of Human Genetics
|
May 6, 2004
Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages
Anthony J Schaeffer, June Chung, Konstantina Heretis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 22, 2008
Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p
Xueya Hauge, Gordana Raca, Sara Cooper, et al.
American Journal of Human Genetics
|
March 5, 2002
The evolutionary origin of human subtelomeric homologies--or where the ends begin
Christa Lese Martin, Andrew Wong, Alyssa Gross, et al.
Page
of 10