Asesoramiento Genético y Genómica Humana
Resultados: Listando 10 de 14 en la página 1 de 2
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Documento
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Año
Genotype-phenotype studies in patients with Hypotonia Infantile with Psychomotor...
Molecular studies in autossomal recessive hearing loss
Genetics of keratoconus: Genetical and molecular study of a Brazilian family
Comparison of clinical heterogeneity among carriers with genetic imbalance on 22q11.2...
Study of genes and genetic variants associated with familial breast cancer: impacts...
Early diagnosis of Prader-Willi syndrome in hypotonic neonates
Study of genetic heterogeneity of deafness by next-generation sequencing
Autism spectrum disorders in FMR1 premutation carriers
Genetic basis of vertebral segmentation defects: genetic and clinical study focused...
Genetic and clinical study of patients with progerioid syndromes
Resultados: Listando 10 de 14 en la página 1 de 2
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