Found: 10
Select item for more details and to access through your institution.
A Novel SRY Mutation Leads to Asymmetric SOX9 Activation and Is Responsible for Mixed 46,XY Gonadal Dysgenesis.
- Published in:
- Hormone Research in Paediatrics, 2012, v. 78, n. 3, p. 188, doi. 10.1159/000336925
- By:
- Publication type:
- Article
Initiation of prenatal genetic diagnosis of chromosomal anomalies in Cameroon
- Published in:
- International Journal of Gynecology & Obstetrics, 2012, v. 116, n. 2, p. 174, doi. 10.1016/j.ijgo.2011.10.006
- By:
- Publication type:
- Article
Observational study of disorders of sex development in Yaounde, Cameroon.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 3, p. 417, doi. 10.1515/jpem-2019-0458
- By:
- Publication type:
- Article
Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 4, p. 454, doi. 10.1038/ejhg.2008.214
- By:
- Publication type:
- Article
Is genetic analysis useful in the routine management of hydatidiform mole?
- Published in:
- 2003
- By:
- Publication type:
- journal article
Clinical, biochemical, and biomolecular aspects of congenital adrenal hyperplasia in a group of Cameroonian children and adolescents.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 6, p. 777, doi. 10.1515/jpem-2021-0696
- By:
- Publication type:
- Article
Challenges in Clinical Diagnosis of Williams-Beuren Syndrome in Sub-Saharan Africans: Case Reports from Cameroon.
- Published in:
- Molecular Syndromology, 2014, v. 5, n. 6, p. 287, doi. 10.1159/000369421
- By:
- Publication type:
- Article
Establishment of permanent cell lines purified from human mesothelioma: morphological aspects, new marker expression and karyotypic analysis.
- Published in:
- Histochemistry & Cell Biology, 2004, v. 122, n. 3, p. 249, doi. 10.1007/s00418-004-0701-1
- By:
- Publication type:
- Article
MECP2 duplication syndrome in a patient from Cameroon.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 4, p. 619, doi. 10.1002/ajmg.a.61510
- By:
- Publication type:
- Article