Found: 6
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Primary hypertrophic osteoarthropathy: Report of two novel genetic variants in the gene in two Mexican patients.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 5, p. 1, doi. 10.1002/mgg3.1176
- By:
- Publication type:
- Article
Bilateral plantar plaques in a patient with Keratitis–ichthyosis–deafness syndrome.
- Published in:
- Australasian Journal of Dermatology, 2020, v. 61, n. 4, p. e458, doi. 10.1111/ajd.13369
- By:
- Publication type:
- Article
The Latin American network for congenital malformation surveillance: ReLAMC.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 4, p. 1078, doi. 10.1002/ajmg.c.31872
- By:
- Publication type:
- Article
Expression profile of microRNAs in the testes of patients with Klinefelter syndrome.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-68294-7
- By:
- Publication type:
- Article
A New Case Report of Traboulsi Syndrome: A Literature Review and Insights Into Genotype–Phenotype Correlations.
- Published in:
- 2024
- By:
- Publication type:
- Case Study