DiGeorge syndrome

06 Oct 15

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Methyltetrahydrofolate reductase (MTHFR)

06 Oct 15

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Medium chain acyl-CoA dehydrogenase (ACADM)

06 Oct 15

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Glucose-6-phosphate dehydrogenase deficiency (G6PD)

06 Oct 15

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Factor XI deficiency (F11)

06 Oct 15

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Creatine (transporter) deficiency (SLC6A8)

06 Oct 15

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Y-chromosome detection (SRY)

06 Oct 15

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CTRC-related hereditary pancreatitis

06 Oct 15

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Cowden syndrome (PTEN)

06 Oct 15

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Costello syndrome (HRAS, KRAS, BRAF)

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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