Application of Clinical Genetics : Impact Factor & More
eISSN: 1178-704XpISSN: 1178-704X
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Key Metrics
CiteScore 
3
SJR
Q3Genetics
SNIP
1
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Topics Covered on Application of Clinical Genetics
Application of Clinical Genetics Journal Specifications
Indexed in the following public directories
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DOAJ 
SJR
| Overview | |
| Publisher | Dove Medical Press |
| Language | English |
| Frequency | Continuous publication |
| Article Processing Charges | USD 2320 |
| Publication Time | 16 |
| Editorial Review Process | Blind peer review |
| General Details | |
| Language | English |
| Frequency | Continuous publication |
| Publication Start Year | 2008 |
| Publisher URL | Visit website |
| Website URL | Visit website |
| Publication Details | |
| Editorial Review Detail | |
| Information for authors | |
| Author instructions | Visit website |
| Copyright Details | Visit website |
| Deposit Policy | Sherpa/Romeo |
| License type | CC BY, CC BY-NC |
| OA statement | Visit website |
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Recently Published Papers in Application of Clinical Genetics
Genetic Polymorphisms of Transforming Growth Factor Receptors (TGF-βRI, TGF-βRII) and Risk Factors Associated with Keloid Scars in Burkina Faso: A Cross-Sectional Study
- 1 May 2026
- The Application of Clinical Genetics
Two Distinct Clinical Presentations of Primary Ciliary Dyskinesia (PCD): Diagnostic Utility of Whole-Exome Sequencing in a Genetically Heterogeneous Disorder
- 2 Apr 2026
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Prenatal Ultrasound and Genetic Diagnosis of EFTUD2 Haploinsufficiency in Two Fetuses: A Case Series
- 27 Mar 2026
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Hearing, Voice and Speech Disorders in 10-Year-Old-Boy with Facio-Scapulo-Humeral Dystrophy (FSHD) – Case Study
- 7 Mar 2026
- The Application of Clinical Genetics
Case Report: Schaaf-Yang Syndrome Milder Phenotype Due to Potential Pathogenic Novel Missense Variant as an Unusual Cause of Obesity in a Pediatric Patient
- 1 Mar 2026
- The Application of Clinical Genetics
Routine Excision, Rare Diagnosis: Solitary Neurofibroma Prompting NF1 Screening in an Adolescent
- 6 Feb 2026
- The Application of Clinical Genetics
Genetic Polymorphisms of Transforming Growth Factor Receptors (TGF-βRI, TGF-βRII) and Risk Factors Associated with Keloid Scars in Burkina Faso: A Cross-Sectional Study
- 1 May 2026
- The Application of Clinical Genetics
Two Distinct Clinical Presentations of Primary Ciliary Dyskinesia (PCD): Diagnostic Utility of Whole-Exome Sequencing in a Genetically Heterogeneous Disorder
- 2 Apr 2026
- The Application of Clinical Genetics
Prenatal Ultrasound and Genetic Diagnosis of EFTUD2 Haploinsufficiency in Two Fetuses: A Case Series
- 27 Mar 2026
- The Application of Clinical Genetics
Hearing, Voice and Speech Disorders in 10-Year-Old-Boy with Facio-Scapulo-Humeral Dystrophy (FSHD) – Case Study
- 7 Mar 2026
- The Application of Clinical Genetics
Case Report: Schaaf-Yang Syndrome Milder Phenotype Due to Potential Pathogenic Novel Missense Variant as an Unusual Cause of Obesity in a Pediatric Patient
- 1 Mar 2026
- The Application of Clinical Genetics
Routine Excision, Rare Diagnosis: Solitary Neurofibroma Prompting NF1 Screening in an Adolescent
- 6 Feb 2026
- The Application of Clinical Genetics
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