DOI: 10.1055/s-00046370

Global Medical Genetics

Ausgabe 01 · Volume 10 · Januar 2023 DOI: 10.1055/s-013-56337

Original Article

  • 001
    Poaty, Henriette; Bouya, Lauria Batamba; Lumaka, Aimé; Mongo-Onkouo, Arnaud; Gassaye, Deby:

    PMS2 Pathogenic Variant in Lynch Syndrome-Associated Colorectal Cancer with Polyps

    Open Access
  • 006
    Khan, Mahamad Irfanulla; C.S, Prashanth; Mustak, Mohammed S.; Nizamuddin, Sheikh:

    Maternal Transmission of the PAX7 Single Nucleotide Polymorphisms among Indian Cleft Trios

    Open Access
  • 012
    Ansari, Neda; Ramachandran, Vasudevan; Mohamad, Nur Afiqah; Salim, Elnaz; Ismail, Patimah; Hazmi, Mohamad; Mat, Liyana Najwa Inchee:

    Association of GCK (rs1799884), GCKR (rs780094), and G6PC2 (rs560887) Gene Polymorphisms with Type 2 Diabetes among Malay Ethnics

    Open Access
  • 22
    Ergoren, Mahmut Cerkez; Akan, Gokce; Guler, Emrah; Tuncel, Gulten; Akovalı, Damla; Evren, Emine Unal; Evren, Hakan; Suer, Huseyin Kaya; Sanlidag, Tamer:

    Sex and ABO Blood Differences in SARS-CoV-2 Infection Susceptibility

    Open Access
  • 027
    Mamurova, Begimai; Akan, Gokce; Mogol, Evren; Turgay, Ayla; Tuncel, Gulten; Evren, Emine Unal; Evren, Hakan; Suer, Kaya; Sanlidag, Tamer; Ergoren, Mahmut Cerkez:

    Strong Association between Vitamin D Receptor Gene and Severe Acute Respiratory Syndrome coronavirus 2 Infectious Variants

    Open Access
  • 034
    Khan, Mahamad Irfanulla; CS, Prashanth; Srinath, N.; Neela, Praveen K.; Mohiuddin, Mohammed K.:

    Genetic Analysis of the Single-Nucleotide Polymorphisms rs880810, rs545793, rs80094639, and rs13251901 in Nonsyndromic Oral Clefts: A Case–Parent Trio Study

    Open Access

    • Rapid Communication

  • 19
    Kanduc, Darja:

    Molecular Mimicry between Respiratory Syncytial Virus F Antigen and the Human Proteome

    Open Access
    Supplementary Material (PDF)

    • Case Report

  • 038
    Alotaibi, Lena; Alqasmi, Amal:

    Identification of a de novo Mutation in TMEM106B in a Saudi Child Causes Hypomyelination Leukodystrophy

    Open Access