Menu
Back to Journals » The Application of Clinical Genetics » Volume 18 » default
ISSN: 1178-704X
- View all (323)
- Volume 18, 2025 (11)
- Volume 17, 2024 (23)
- Volume 16, 2023 (20)
- Volume 15, 2022 (16)
- Volume 14, 2021 (37)
- Volume 13, 2020 (23)
- Volume 12, 2019 (30)
- Volume 11, 2018 (23)
- Volume 10, 2017 (12)
- Volume 9, 2016 (22)
- Volume 8, 2015 (24)
- Volume 7, 2014 (23)
- Volume 6, 2013 (12)
- Volume 5, 2012 (13)
- Volume 4, 2011 (14)
- Volume 3, 2010 (15)
- Volume 2, 2009 (2)
- Volume 1, 2008 (3)
Archive: Volume 18, 2025
The Impact of FSHR Polymorphisms (rs6165 and rs6166) on Ovarian Response to Stimulation in Infertile Women with Diminished Ovarian Reserve
Hoang TTT, Trinh ST, Nguyen NN, Ho MN, Pham MD, Hoang NT, Trieu ST, Ho HS
The Application of Clinical Genetics 2025, 18:119-129
Published Date: 12 July 2025
Coexistence of Hereditary Hemorrhagic Telangiectasia and Moyamoya Disease: A Case Report Highlighting a Potential Genetic Synergy
Liu S, Meng L, Wan Y, Liu S, Shi L
The Application of Clinical Genetics 2025, 18:113-117
Published Date: 10 July 2025
A Systematic Review of SNPs Screening for Platinum-Related Pharmacodynamics and Pharmacokinetics Genes in Non-Small Cell Lung Cancer for Precision Medicine
Afifah NN, Larasati AL, Wijaya I, Zakiyah N, Intania R, Obinata H, Barliana MI
The Application of Clinical Genetics 2025, 18:93-112
Published Date: 27 June 2025
Genetic Polymorphisms and QF-PCR Performance Evaluation of 20 Autosomal STR Loci on Chromosomes 13, 18, and 21 in Prenatal Diagnosis Among East Chinese Han Population
Liu Y, Xue J, Yan L, Chen C, Zhao S, Li H
The Application of Clinical Genetics 2025, 18:81-91
Published Date: 12 June 2025
Intramuscular Vitamin B12 Treatment in Transcobalamin II Deficiency: Case Series Clinical Outcomes
Sawlan AM, Alotaibi M, Alharbi RM, Alwahbi NA, Alshammary M, Alasmari AM, Al Mutairi F
The Application of Clinical Genetics 2025, 18:73-80
Published Date: 5 June 2025
A Novel EBP c.452A>G Mutation Identified in a Girl with Conradi–Hünermann–Happle Syndrome Presenting with Hydronephrosis
Qiao F, Zeng H, Zhang C, Wang Y, Wang Y, Zhou R, Meng L, Hu P, Xu Z
The Application of Clinical Genetics 2025, 18:63-72
Published Date: 14 May 2025
The Frequency of CYP2C19*2 Gene Polymorphisms in Burkina Faso Patients Treated with Clopidogrel
Kagambèga YD, Ouattara AK, Ouédraogo TWC, Traoré L, Yaméogo NV, Simpore J
The Application of Clinical Genetics 2025, 18:55-61
Published Date: 1 May 2025
NIPT of Maternal Plasma-Originated cfDNA: Applications and Guide for the Implementation
Fernández Martínez FJ, Gil Mira MM, González González C, Madrigal Bajo I, Oancea Ionescu R, Orellana Alonso C
The Application of Clinical Genetics 2025, 18:41-53
Published Date: 26 April 2025
Survey of Structural Autosomal Abnormalities and Autosomal Variants in Infertile Patients Treated at Some IVF Centers in Vietnam
Trieu ST, Pham MD, Le H, Vo HV, Nguyen PV, Tran TV, Nguyen NN, Trinh ST
The Application of Clinical Genetics 2025, 18:29-40
Published Date: 11 April 2025
Associations of Karyotype and Age at Diagnosis with Physical Features and Comorbidities in Turner Syndrome: A Single-Site Experience
Vida B, Török O, Felszeghy E, Orosz M, Krasznai ZT, Tándor Z, Jakab A, Deli T
The Application of Clinical Genetics 2025, 18:9-27
Published Date: 14 February 2025
Vascular Pathology in Alpha 1 Antitrypsin Deficient Chronic Obstructive Pulmonary Disease and Emphysema Patients: Case Reports
Gordon M, Gangemi AJ, Sandwith EL, Kumaran M, Kueppers F
The Application of Clinical Genetics 2025, 18:1-7
Published Date: 28 January 2025