Asesoramiento Genético y Genómica Humana
Resultados: Listando 10 de 17 en la página 1 de 2
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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...
Functional assessment of human embryos donated for research: viability, morphological...
Investigation of extreme skewing of X-chromosome inactivation in women with idiopathic...
Clinical data for interpretation of secondary genomic findings in elderly people...
Early diagnosis of Prader-Willi syndrome in hypotonic neonates
Study of genetic heterogeneity of deafness by next-generation sequencing
Resultados: Listando 10 de 17 en la página 1 de 2
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