Rett syndrome (classic, atypical, and congenital variants) panel

06 Oct 15

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Rett syndrome – congenital variant form (FOXG1)

06 Oct 15

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Rett syndrome – atypical (STK9/CDKL5)

06 Oct 15

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Rett syndrome (MECP2)

06 Oct 15

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Retinitis pigmentosa sequencing panel (66 gene)

06 Oct 15

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Renpenning syndrome (PQBP1)

06 Oct 15

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PTCHD1 (X-linked intellectual disability/ autism spectrum disorder)

06 Oct 15

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PRSS1-Related hereditary pancreatitis

06 Oct 15

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Prothrombin (20210G˃A mutation)

06 Oct 15

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Proteus syndrome (PTEN)

06 Oct 15

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La mutación G202A, en hijo hemicigoto (arriba) y madre heterocigota (abajo). Esta mutación acompañada de la mutación A376G ó T968C definen la variante africana negativa.

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Arriba se muestra el resultado de un niño hemicigoto para la variante africana negativa, caracterizada por las mutaciones A376G y G202A, y abajo de una niña heterocigota para la variante Mediterránea, definida por la mutación C563T.

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The G202A mutation, in the hemizygous son (above) and heterozygous mother (below). This
mutation accompanied with the A376G mutation or T968C define the african negative variant.

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Above the result of a hemizygous child with the african negative variant , characterized by
mutations A376G and G202A , and below a heterozygous girl with the mediterranean variant, defined by the C563T mutation

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