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MTSS2-related neurodevelopmental disorder: Further delineation of the phenotype.
Eur J Med Genet. 2023 Oct;66(10):104826. doi: 10.1016/j.ejmg.2023.104826. Epub 2023 Aug 30.
Eur J Med Genet. 2023.
PMID: 37657631
Aneurysms involving the coronary arteries in a neonate with neurofibromatosis 1.
Corona-Rivera JR, Barrios-Prieto E, Rivera-Ramírez B, Sánchez-Uribe EH, Cortés-Pastrana RC, Aguilera CER, de Anda-Camacho RG, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A.
Corona-Rivera JR, et al. Among authors: cortes pastrana rc.
Am J Med Genet A. 2023 Sep;191(9):2422-2427. doi: 10.1002/ajmg.a.63321. Epub 2023 Jun 6.
Am J Med Genet A. 2023.
PMID: 37278515
Review.
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Intrafamilial variability and neurological manifestations in two siblings with carbohydrate sulfotransferase 3-related skeletal dysplasia.
Rivera-Vargas J, Superti-Furga A, Bonafé L, Peña-Padilla C, Cortés-Pastrana RC, Bobadilla-Morales L, Corona-Rivera A, Corona-Rivera JR.
Rivera-Vargas J, et al. Among authors: cortes pastrana rc.
Clin Dysmorphol. 2023 Jan 1;32(1):14-17. doi: 10.1097/MCD.0000000000000432. Epub 2022 Sep 12.
Clin Dysmorphol. 2023.
PMID: 36503918
No abstract available.
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