Asesoramiento Genético y Genómica Humana
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Genetics of keratoconus: Genetical and molecular study of a Brazilian family
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 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...
Myotubular myopathy: molecular diagnosis and genetic counselling in Brazilian fa...
Next generation sequencing and its application on the genetic study of Waardenburg...
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Resultados: Listando 10 de 10 en la página 1 de 1
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