Works matching IS 1178704X AND DT 2022 AND VI 15
Results: 16
HLA-DQA1 and HLA-DQB1 Gene Polymorphism in Indonesian Children with Type I Diabetes Mellitus.
- Published in:
- Application of Clinical Genetics, 2022, v. 15, p. 11, doi. 10.2147/TACG.S348115
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- Publication type:
- Article
Long Non-Coding RNAs ASB16-AS1 and AFAP1-AS1: Diagnostic, Prognostic Impact and Survival Analysis in Colorectal Cancer.
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- Application of Clinical Genetics, 2022, v. 15, p. 97, doi. 10.2147/TACG.S370242
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- Article
ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy.
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- Application of Clinical Genetics, 2022, v. 15, p. 111, doi. 10.2147/TACG.S359479
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- Publication type:
- Article
Utility of Measuring Fetal Cavum Septum Pellucidum (CSP) Width During Routine Obstetrical Ultrasound for Improving Diagnosis of 22q11.2 Deletion Syndrome: A Case-Control Study.
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- Application of Clinical Genetics, 2022, v. 15, p. 87, doi. 10.2147/TACG.S364543
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- Publication type:
- Article
Deregulation of CircANXA2, Circ0075001, and CircFBXW7 Gene Expressions and Their Predictive Value in Egyptian Acute Myeloid Leukemia Patients.
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- Application of Clinical Genetics, 2022, v. 15, p. 69, doi. 10.2147/TACG.S365613
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- Article
A Novel POGZ Variant in a Patient with Intellectual Disability and Obesity.
- Published in:
- 2022
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- Publication type:
- Case Study
Evaluating the Association Between Genetic Polymorphisms Related to Homocysteine Metabolism and Unexplained Recurrent Pregnancy Loss in Women.
- Published in:
- Application of Clinical Genetics, 2022, v. 15, p. 55, doi. 10.2147/TACG.S365281
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- Publication type:
- Article
Prominent Mutation of Intron 22 Inversion in Sporadic Hemophilia: Is It Worth the Antenatal Screening?
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- Application of Clinical Genetics, 2022, v. 15, p. 49, doi. 10.2147/TACG.S363132
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- Publication type:
- Article
Molecular Genetic Screening of Neonatal Intensive Care Units: Hyperbilirubinemia as an Example.
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- Application of Clinical Genetics, 2022, v. 15, p. 39, doi. 10.2147/TACG.S362148
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- Publication type:
- Article
Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor Retardation.
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- Application of Clinical Genetics, 2022, v. 15, p. 27, doi. 10.2147/TACG.S357136
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- Publication type:
- Article
CTLA-4 CT-60 A/G and CTLA-4 1822 C/T Gene Polymorphisms in Indonesians with Type 1 Diabetes Mellitus.
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- Application of Clinical Genetics, 2022, v. 15, p. 19, doi. 10.2147/TACG.S359158
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- Publication type:
- Article
Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome.
- Published in:
- 2022
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- Publication type:
- Case Study
RASopathy Cohort of Patients Enrolled in a Brazilian Reference Center for Rare Diseases: A Novel Familial LZTR1 Variant and Recurrent Mutations.
- Published in:
- Application of Clinical Genetics, 2022, v. 15, p. 153, doi. 10.2147/TACG.S372761
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- Publication type:
- Article
Three-Decade Successive Establishment of Care for Women/Girls from Families with Haemophilia.
- Published in:
- Application of Clinical Genetics, 2022, v. 15, p. 133, doi. 10.2147/TACG.S381683
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- Publication type:
- Article
Prenatal Sonographic Features of Rare Chromosome 13 Aberrations.
- Published in:
- Application of Clinical Genetics, 2022, v. 15, p. 145, doi. 10.2147/TACG.S370163
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- Publication type:
- Article
Case Report of a Juvenile Patient with Autism Spectrum Disorder with a Novel Combination of Copy Number Variants in ADGRL3 (LPHN3) and Two Pseudogenes.
- Published in:
- 2022
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- Publication type:
- Case Study