Asesoramiento Genético y Genómica Humana
Resultados: Listando 10 de 21 en la página 2 de 3
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Año
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...
X-linked intellectual disability: study of sibships with two or more affected brothers...
Genetic and clinical study of patients with progerioid syndromes
Clinical and genetic investigation of ataxia with vitamin E deficiency (AVED), a...
From top to bottom: genetic counseling in families ascertained through fragile X-associated...
Syndromic intellectual disability diagnosis by next-generation sequencing in consanguineous...
Myotubular myopathy: molecular diagnosis and genetic counselling in Brazilian fa...
Resultados: Listando 10 de 21 en la página 2 de 3
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