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Search Results - Alvarez‐Mora, M.I.
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Fragile X syndrome: An overview and update of the FMR1 gene
by
Mila, M.
,
Alvarez‐Mora, M.I.
,
Madrigal, I.
,
Rodriguez‐Revenga, L.
Published in
Clinical genetics
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Spectrum of clinical heterogeneity of β-tubulin TUBB5 gene mutations
by
Madrigal, I.
,
Rabionet, R.
,
Alvarez-Mora, M.I.
,
Sanchez, A.
,
Rodríguez-Revenga, L.
,
Estivill, X.
,
Mila, M.
Published in
Gene
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Clinical implication of FMR1 intermediate alleles in a Spanish population
by
Alvarez‐Mora, M.I.
,
Madrigal, I.
,
Martinez, F.
,
Tejada, M.‐I.
,
Izquierdo‐Alvarez, S.
,
Sanchez‐Villar de Saz, P.
,
Caro‐Llopis, A.
,
Villate, O.
,
Rodríguez‐Santiago, B.
,
Pérez Jurado, L.A.
,
Rodriguez‐Revenga, L.
,
Milà, M.
Published in
Clinical genetics
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Social anxiety and autism spectrum traits among adult FMR1 premutation carriers
by
López‐Mourelo, O.
,
Mur, E.
,
Madrigal, I.
,
Alvarez‐Mora, M.I.
,
Gómez‐Ansón, B.
,
Pagonabarraga, J.
,
Rodriguez‐Revenga, L.
,
Milà, M.
Published in
Clinical genetics
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Clinical Genetics
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Gene
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Genetics & Heredity
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Life Sciences & Biomedicine
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Science & Technology
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Ataxia
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Autism
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Fmr1 Protein
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Fragile X Syndrome
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Fxtas
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Genetic Counseling
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Intellectual Disabilities
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Tremor
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Adult
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Aged
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Alleles
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Anxiety
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Anxiety Disorders - Genetics
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