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American Journal of Medical Genetics. Part A
|
November 18, 2008
Microarray-based DNA methylation analysis of imprinted loci in a patient with transient neonatal diabetes mellitus
Jose I Martin-Subero, Marina Bibikova, Deborah Mackay, et al.
American Journal of Medical Genetics. Part A
|
August 6, 2003
No mutation in the gene for Noonan syndrome, PTPN11, in 18 patients with Costello syndrome
Birte Tröger, Kerstin Kutsche, Hanno Bolz, et al.
American Journal of Medical Genetics. Part A
|
August 6, 2013
Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders
Rebecca L Poole, Louise E Docherty, Abeer Al Sayegh, et al.
Archives of Gynecology and Obstetrics
|
May 17, 2013
Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies
Andreas Roos, Constantin S von Kaisenberg, Thomas Eggermann, et al.
European Journal of Human Genetics : EJHG
|
December 13, 2012
Frequency and characterization of DNA methylation defects in children born SGA
Susanne Bens, Andrea Haake, Julia Richter, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 11, 2019
Reduced Androgen Receptor Expression in Genital Skin Fibroblasts From Patients With 45,X/46,XY Mosaicism
Nadine C Hornig, Jeta Demiri, Pascal Rodens, et al.
American Journal of Medical Genetics. Part A
|
April 29, 2010
Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1
Diana Mitter, Barbara Delle Chiaie, Hermann-Josef Lüdecke, et al.
Clinical Epigenetics
|
June 13, 2019
DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMs
Kirstin Hoff, Marta Lemme, Anne-Karin Kahlert, et al.
Molecular Genetics & Genomic Medicine
|
October 6, 2015
Mutations in CDK5RAP2 cause Seckel syndrome
Gökhan Yigit, Karen E Brown, Hülya Kayserili, et al.
Scientific Reports
|
July 15, 2024
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome
Jelena Pozojevic, Radhika Sivaprasad, Joshua Laß, et al.
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of 9
Search research articles
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Showing results (41-50 of 81) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics. Part A
|
November 18, 2008
Microarray-based DNA methylation analysis of imprinted loci in a patient with transient neonatal diabetes mellitus
Jose I Martin-Subero, Marina Bibikova, Deborah Mackay, et al.
American Journal of Medical Genetics. Part A
|
August 6, 2003
No mutation in the gene for Noonan syndrome, PTPN11, in 18 patients with Costello syndrome
Birte Tröger, Kerstin Kutsche, Hanno Bolz, et al.
American Journal of Medical Genetics. Part A
|
August 6, 2013
Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders
Rebecca L Poole, Louise E Docherty, Abeer Al Sayegh, et al.
Archives of Gynecology and Obstetrics
|
May 17, 2013
Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies
Andreas Roos, Constantin S von Kaisenberg, Thomas Eggermann, et al.
European Journal of Human Genetics : EJHG
|
December 13, 2012
Frequency and characterization of DNA methylation defects in children born SGA
Susanne Bens, Andrea Haake, Julia Richter, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 11, 2019
Reduced Androgen Receptor Expression in Genital Skin Fibroblasts From Patients With 45,X/46,XY Mosaicism
Nadine C Hornig, Jeta Demiri, Pascal Rodens, et al.
American Journal of Medical Genetics. Part A
|
April 29, 2010
Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1
Diana Mitter, Barbara Delle Chiaie, Hermann-Josef Lüdecke, et al.
Clinical Epigenetics
|
June 13, 2019
DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMs
Kirstin Hoff, Marta Lemme, Anne-Karin Kahlert, et al.
Molecular Genetics & Genomic Medicine
|
October 6, 2015
Mutations in CDK5RAP2 cause Seckel syndrome
Gökhan Yigit, Karen E Brown, Hülya Kayserili, et al.
Scientific Reports
|
July 15, 2024
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome
Jelena Pozojevic, Radhika Sivaprasad, Joshua Laß, et al.
Page
of 9