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| 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 |