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American Journal of Medical Genetics. Part A
|
March 8, 2026
Revisiting the W-Index and Waardenburg Syndrome: A Retrospective Review of Waardenburg Syndrome Diagnoses at a Single Site Hearing Loss Clinic and the Sensitivity, Specificity, and Genotype-Phenotype Correlations of an Elevated W-Index
Kyle Mahoney, Kelsey Crocker, Justin Blair, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Congenital heart disease in Cornelia de Lange syndrome: phenotype and genotype analysis
Kathryn C Chatfield, Samantha A Schrier, Jennifer Li, et al.
Scientific Reports
|
May 21, 2026
A robust direction of arrival estimation method based on the chaotic MUSIC algorithm
Bijaya Kumar Muni, Tahesin Samira Delwar, Trilochan Panigrahi, et al.
American Journal of Human Genetics
|
August 20, 2004
NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations
Lynette A Gillis, Jennifer McCallum, Maninder Kaur, et al.
Tuberculosis (Edinburgh, Scotland)
|
March 10, 2026
Vitreous transcriptomic profiling reveals miR-4762 as a potential diagnostic biomarker and modulator of disease pathophysiology in Tubercular Uveitis
Kritika Kakkar, Maninder Kaur, Vishali Gupta, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
April 28, 2016
Characterization of limb differences in children with Cornelia de Lange Syndrome
Devanshi Mehta, Samantha A Schrier Vergano, Matthew Deardorff, et al.
Nature Communications
|
May 19, 2021
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
Felix D Weiss, Lesly Calderon, Yi-Fang Wang, et al.
American Journal of Medical Genetics. Part A
|
November 22, 2012
Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome
Laura K Conlin, Maninder Kaur, Kosuke Izumi, et al.
Scientific Reports
|
January 20, 2018
NIPBL<sup>+/-</sup> haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states
Jason A Mills, Pamela S Herrera, Maninder Kaur, et al.
Journal of Periodontology
|
December 17, 2020
Evaluating efficacy of a novel dentifrice in reducing probing depths in Stage I and II periodontitis maintenance patients: A randomized, double-blind, positive controlled clinical trial
Maninder Kaur, Nicolaas C Geurs, Charles M Cobb, et al.
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of 25
Search research articles
Search
Showing results (201-210 of 241) with videos related to
Sort By:
Page
of 25
American Journal of Medical Genetics. Part A
|
March 8, 2026
Revisiting the W-Index and Waardenburg Syndrome: A Retrospective Review of Waardenburg Syndrome Diagnoses at a Single Site Hearing Loss Clinic and the Sensitivity, Specificity, and Genotype-Phenotype Correlations of an Elevated W-Index
Kyle Mahoney, Kelsey Crocker, Justin Blair, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Congenital heart disease in Cornelia de Lange syndrome: phenotype and genotype analysis
Kathryn C Chatfield, Samantha A Schrier, Jennifer Li, et al.
Scientific Reports
|
May 21, 2026
A robust direction of arrival estimation method based on the chaotic MUSIC algorithm
Bijaya Kumar Muni, Tahesin Samira Delwar, Trilochan Panigrahi, et al.
American Journal of Human Genetics
|
August 20, 2004
NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations
Lynette A Gillis, Jennifer McCallum, Maninder Kaur, et al.
Tuberculosis (Edinburgh, Scotland)
|
March 10, 2026
Vitreous transcriptomic profiling reveals miR-4762 as a potential diagnostic biomarker and modulator of disease pathophysiology in Tubercular Uveitis
Kritika Kakkar, Maninder Kaur, Vishali Gupta, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
April 28, 2016
Characterization of limb differences in children with Cornelia de Lange Syndrome
Devanshi Mehta, Samantha A Schrier Vergano, Matthew Deardorff, et al.
Nature Communications
|
May 19, 2021
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
Felix D Weiss, Lesly Calderon, Yi-Fang Wang, et al.
American Journal of Medical Genetics. Part A
|
November 22, 2012
Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome
Laura K Conlin, Maninder Kaur, Kosuke Izumi, et al.
Scientific Reports
|
January 20, 2018
NIPBL<sup>+/-</sup> haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states
Jason A Mills, Pamela S Herrera, Maninder Kaur, et al.
Journal of Periodontology
|
December 17, 2020
Evaluating efficacy of a novel dentifrice in reducing probing depths in Stage I and II periodontitis maintenance patients: A randomized, double-blind, positive controlled clinical trial
Maninder Kaur, Nicolaas C Geurs, Charles M Cobb, et al.
Page
of 25