Maria Juliana
Ballesta Martinez
Asociado Ciencias de la Salud
Centro de Investigación Biomédica en Red sobre Enfermedades Raras
Madrid, EspañaPublications in collaboration with researchers from Centro de Investigación Biomédica en Red sobre Enfermedades Raras (10)
2024
-
Identification of copy-number variants in patients with overgrowth disorders
Clinical Genetics, Vol. 106, Núm. 5, pp. 614-624
2023
-
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene
International Journal of Molecular Sciences, Vol. 24, Núm. 2
-
Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature
Genes, Vol. 14, Núm. 6
2022
-
Extremely variable expressivity in Smith-Lemli-Opitz syndrome: Review of 4 cases
Anales de Pediatria, Vol. 96, Núm. 3, pp. 253-255
2020
-
Assessment of psychomotor development of Spanish children up to 3 years of age conceived by assisted reproductive techniques: Prospective matched cohort study
Anales de Pediatria, Vol. 92, Núm. 4, pp. 200-207
-
First Spanish case of syndromic intellectual disability with dysmorphic facies, seizures, and distal limb anomalies caused by balletic mutations in the OTUD6B gene
Anales de Pediatria, Vol. 92, Núm. 3, pp. 169-171
2017
-
Molecular spectrum and differential diagnosis in patients referred with sporadic or autosomal recessive osteogenesis imperfecta
Molecular Genetics and Genomic Medicine, Vol. 5, Núm. 1, pp. 28-39
2016
-
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
Genetics in Medicine, Vol. 18, Núm. 12, pp. 1226-1234
2015
-
Identification of the fourth duplication of upstream IHH regulatory elements, in a family with craniosynostosis Philadelphia type, helps to define the phenotypic characterization of these regulatory elements
American Journal of Medical Genetics, Part A, Vol. 167, Núm. 4, pp. 902-906
2014
-
Two mutations in IFITM5 causing distinct forms of osteogenesis imperfecta
American Journal of Medical Genetics, Part A, Vol. 164, Núm. 5, pp. 1136-1142