BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Minatogawa M, Unzaki A, Morisaki H, et al. (2021) Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in (mcEDS-). Journal of Medical Genetics |
Aguayo-Orozco TA, Ríos-González BE, Castro-Martínez AG, et al. (2020) Generalized hypertrichosis syndromes in Mexico. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics |
Ramírez-Velazco A, Aguayo-Orozco TA, Figuera L, et al. (2019) Williams-Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH. Journal of Genetics. 98 |
Domínguez MG, Rivera H, Aguilar-Lemarroy A, et al. (2017) Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring. Clinical Dysmorphology |
Becerra-Solano LE, Arnaud-Lopez L, Diaz-Rodriguez M, et al. (2008) First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patient. Clinical Dysmorphology. 17: 27-30 |
Vásquez-Velásquez AI, Arnaud-López L, Figuera LE, et al. (2005) Ambiguous genitalia by 9p deletion inherent to a dic(Y;9)(q12;p24). Journal of Applied Genetics. 46: 415-8 |