American Journal of Medical Genetics, Part C: Seminars in Medical Genetics : Impact Factor & More
eISSN: 1552-4876pISSN: 1552-4868
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Key Metrics
CiteScore 
5.5
Impact Factor
< 5
SNIP
1.58
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American Journal of Medical Genetics, Part C: Seminars in Medical Genetics Journal Specifications
| Overview | |
| Publisher | WILEY |
| Language | English |
| Frequency | Quarterly |
| General Details | |
| Language | English |
| Frequency | Quarterly |
| Publication Start Year | 1977 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
A Novel Splice Variant in ERGIC1 Causes Arthrogryposis Multiplex Congenita-Characterization Using Urine-Derived Cells.
- 15 May 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Spectrum of Congenital Anomalies in Myhre Syndrome-Insights Into Effects Brought by Altered TGF-β Signaling via Gain-of-Function Variants in SMAD4.
- 13 Apr 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profileand Associated Factors.
- 16 Mar 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Therapy for Myhre Syndrome: Goals, Misconceptions, and Current Agents.
- 16 Mar 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Review of Cutaneous Manifestations in Myhre Syndrome With Histopathological Analyses and Genotype-Phenotype Correlation.
- 12 Feb 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Unraveling the Mechanistic Spectrum of Myhre Syndrome: SMAD4 Signaling Disruption, Skeletal Phenotypes, and Translational Innovation.
- 8 Feb 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
A Novel Splice Variant in ERGIC1 Causes Arthrogryposis Multiplex Congenita-Characterization Using Urine-Derived Cells.
- 15 May 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Spectrum of Congenital Anomalies in Myhre Syndrome-Insights Into Effects Brought by Altered TGF-β Signaling via Gain-of-Function Variants in SMAD4.
- 13 Apr 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profileand Associated Factors.
- 16 Mar 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Therapy for Myhre Syndrome: Goals, Misconceptions, and Current Agents.
- 16 Mar 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Review of Cutaneous Manifestations in Myhre Syndrome With Histopathological Analyses and Genotype-Phenotype Correlation.
- 12 Feb 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
Unraveling the Mechanistic Spectrum of Myhre Syndrome: SMAD4 Signaling Disruption, Skeletal Phenotypes, and Translational Innovation.
- 8 Feb 2026
- American journal of medical genetics. Part C, Seminars in medical genetics
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