Works matching IS 26999404 AND DT 2022 AND VI 9 AND IP 1

Results: 11

Clinical Features of Aberrations Chromosome 22q: A Pilot Study.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 42, doi. 10.1055/s-0041-1739496

By:

Atli, Emine Ikbal;
Atli, Engin;
Yalcintepe, Sinem;
Demir, Selma;
Mail, Cisem;
Eker, Damla;
Ozen, Yasemin;
Gurkan, Hakan

Publication type:

Article

FromGenetics to Epigenetics: Top 4 Aspects for Improved SARS-CoV-2 Vaccine Designs as Paradigmatic Examples.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 14, doi. 10.1055/s-0041-1739495

By:

Kanduc, Darja

Publication type:

Article

Epigenetic Approach to PTSD: In the Aspects of Rat Models.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 7, doi. 10.1055/s-0041-1736633

By:

Aykac, Asli;
Kalkan, Rasime

Publication type:

Article

Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 34, doi. 10.1055/s-0041-1736567

By:

Ganaraja, Valakunja H.;
Polavarapu, Kiran;
Bardhan, Mainak;
Preethish-Kumar, Veeramani;
Leena, Shingavi;
Anjanappa, Ram M.;
Vengalil, Seena;
Nashi, Saraswati;
Arunachal, Gautham;
Gunasekaran, Swetha;
Mohan, Dhaarini;
Raju, Sanita;
Unnikrishnan, Gopikrishnan;
Huddar, Akshata;
Ravi-Kiran, Valasani;
Thomas, Priya T.;
Nalini, Atchayaram

Publication type:

Article

Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 29, doi. 10.1055/s-0041-1736566

By:

Atli, Emine Ikbal;
Atli, Engin;
Yalcintepe, Sinem;
Demir, Selma;
Kalkan, Rasime;
Akurut, Cisem;
Ozen, Yasemin;
Gurkan, Hakan

Publication type:

Article

A New Perspective of COVID-19 Infection: An Epigenetics Point of View.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 4, doi. 10.1055/s-0041-1736565

By:

Ozturkler, Ziya;
Kalkan, Rasime

Publication type:

Article

Toe Walking as the Initial Symptom of a Spinocerebellar Ataxia 13 in a Patient Presenting with a Mutation in the KCNC3 Gene.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 51, doi. 10.1055/s-0041-1736483

By:

Pomarino, David;
Thren, Johanna Ronja;
Thren, Anneke;
Rostasy, Kevin;
Schoenfeldt, Jan

Publication type:

Article

Rare Findings in Cleidocranial Dysplasia Caused by RUNX Mutation.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 23, doi. 10.1055/s-0041-1736482

By:

Yigin, Aysel Kalayci;
Duz, Mehmet Bugrahan;
Seven, Mehmet

Publication type:

Article

Alpelisib: A Well-Tolerated Treatment Option for Patients with HR-Positive, HER2-Negative, PIK3CA-Mutated Advanced Breast Cancer.

Published in:

2022

By:

Fei-Yu Diao

Publication type:

Editorial

Genetic Analysis of Neuroligin 4YGene in Autism Population of India.

Published in:

Global Medical Genetics, 2022, v. 9, n. 1, p. 18, doi. 10.1055/s-0041-1736236

By:

Hegde, Rajat;
Hegde, Smita;
Kulkarni, Suyamindra S.;
Pandurangi, Aditya;
Gai, Pramod B.;
Das, Kusal K.

Publication type:

Article

Variant Curation is Crucial to Claim Digenic Inheritance in Juvenile Open Angle Glaucoma.

Published in:

2022

By:

Kok-Siong Poon;
Karen Mei-Ling Tan

Publication type:

Letter to the Editor