Huntington disease(HD, HTT, IT15)

06 Oct 15

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Maternal Cell Contamination (MCC) studies

06 Oct 15

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Coffin-Lowry syndrome (RSK2/RPS6KA3)

06 Oct 15

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COBAS- HPV- 15 high risk genotypes

06 Oct 15

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Clostridium difficile PCR

06 Oct 15

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Zygosity testing

06 Oct 15

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Chudley-Lowry syndrome (ATRX)

06 Oct 15

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Chlamydia trachomatis-PCR

06 Oct 15

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Charge syndrome (CHD7)

06 Oct 15

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Charcot-Marie-Tooth disease, Types 1B, 2I, 2J (MPZ)

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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