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World Journal of Gastrointestinal Pharmacology and Therapeutics
|
September 21, 2020
Role of telomere shortening in anticipation of inflammatory bowel disease
Brindusa Truta, Elizabeth Wohler, Nara Sobreira, et al.
American Journal of Medical Genetics. Part A
|
March 19, 2011
An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy
Gerald Raymond, Elizabeth Wohler, Carolyn Dinsmore, et al.
Case Reports in Genetics
|
December 15, 2015
The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
Molly B Sheridan, Elizabeth Wohler, Denise A S Batista, et al.
American Journal of Medical Genetics. Part A
|
November 8, 2024
Ring Chromosome 17 Syndrome-A Case Report and Discussion of Diagnostic Methods
Sun Young Kim, Elizabeth Wohler, Maria Jimena Gutierrez, et al.
European Journal of Medical Genetics
|
December 15, 2010
Unbalanced translocation 9;16 in two children with dysmorphic features, and severe developmental delay: Evidence of cross-over within derivative chromosome 9 in patient #1
Regina M Zambrano, Elizabeth Wohler, Göran Annerén, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
July 1, 2020
Familial Aggregation in Idiopathic Subglottic Stenosis
Virginia E Drake, Alexander Gelbard, Nara Sobriera, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 15, 2014
The impact of chromosomal microarray on clinical management: a retrospective analysis
Lindsay B Henderson, Carolyn D Applegate, Elizabeth Wohler, et al.
American Journal of Medical Genetics. Part A
|
January 30, 2023
Genetic testing in the evaluation of individuals with clinical diagnosis of atypical Sturge-Weber syndrome
SangEun Yeom, Bernard Cohen, Clifford R Weiss, et al.
The Laryngoscope
|
February 2, 2023
Human Leukocyte Antigen Genotyping of Idiopathic Subglottic Stenosis
Matthew L Rohlfing, Alexander T Hillel, Elizabeth Wohler, et al.
Journal of Medical Genetics
|
November 25, 2010
Mosaic trisomy 13: understanding origin using SNP array
Natini Jinawath, Regina Zambrano, Elizabeth Wohler, et al.
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Search research articles
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Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
World Journal of Gastrointestinal Pharmacology and Therapeutics
|
September 21, 2020
Role of telomere shortening in anticipation of inflammatory bowel disease
Brindusa Truta, Elizabeth Wohler, Nara Sobreira, et al.
American Journal of Medical Genetics. Part A
|
March 19, 2011
An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy
Gerald Raymond, Elizabeth Wohler, Carolyn Dinsmore, et al.
Case Reports in Genetics
|
December 15, 2015
The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
Molly B Sheridan, Elizabeth Wohler, Denise A S Batista, et al.
American Journal of Medical Genetics. Part A
|
November 8, 2024
Ring Chromosome 17 Syndrome-A Case Report and Discussion of Diagnostic Methods
Sun Young Kim, Elizabeth Wohler, Maria Jimena Gutierrez, et al.
European Journal of Medical Genetics
|
December 15, 2010
Unbalanced translocation 9;16 in two children with dysmorphic features, and severe developmental delay: Evidence of cross-over within derivative chromosome 9 in patient #1
Regina M Zambrano, Elizabeth Wohler, Göran Annerén, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
July 1, 2020
Familial Aggregation in Idiopathic Subglottic Stenosis
Virginia E Drake, Alexander Gelbard, Nara Sobriera, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 15, 2014
The impact of chromosomal microarray on clinical management: a retrospective analysis
Lindsay B Henderson, Carolyn D Applegate, Elizabeth Wohler, et al.
American Journal of Medical Genetics. Part A
|
January 30, 2023
Genetic testing in the evaluation of individuals with clinical diagnosis of atypical Sturge-Weber syndrome
SangEun Yeom, Bernard Cohen, Clifford R Weiss, et al.
The Laryngoscope
|
February 2, 2023
Human Leukocyte Antigen Genotyping of Idiopathic Subglottic Stenosis
Matthew L Rohlfing, Alexander T Hillel, Elizabeth Wohler, et al.
Journal of Medical Genetics
|
November 25, 2010
Mosaic trisomy 13: understanding origin using SNP array
Natini Jinawath, Regina Zambrano, Elizabeth Wohler, et al.
Page
of 5