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Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion.
Update and audit of the St George’s classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis.
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins(1;8)(p22.1;q22q23).

Joann Harris

Measles Virus and Rubella Virus Real Time RT PCR Kit

February 2, 2020February 2, 2020 by Joann Harris

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GPER Lentiviral Vector Human pLenti GIII

February 2, 2020 by Joann Harris

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Dog Placenta cDNA

February 2, 2020 by Joann Harris

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Guinea Pig Uterus cDNA

February 2, 2020 by Joann Harris

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Hamster Bladder cDNA

February 2, 2020 by Joann Harris

Hamster Bladder cDNA

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Pig Heart cDNA

February 2, 2020 by Joann Harris

Pig Heart cDNA

Pig Heart cDNA

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Lentiviral Vector Human pLenti

February 2, 2020 by Joann Harris

Lentiviral Vector Human pLenti

Lentiviral Vector Human pLenti

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HCV PCR Seroconversion control

February 2, 2020 by Joann Harris

HCV PCR Seroconversion

HCV PCR Seroconversion control

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Genetic characteristics of non-familial epilepsy.
Genomic variant sharing: a position statement.
Suspected Brugada Phenocopy Secondary to Coronary Slow Flow.

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Genetic characteristics of non-familial epilepsy.
Genomic variant sharing: a position statement.
Suspected Brugada Phenocopy Secondary to Coronary Slow Flow.
Aurion
101 Biosystem

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Genetic characteristics of non-familial epilepsy. Genomic variant sharing: a position statement. Suspected Brugada Phenocopy Secondary to Coronary Slow Flow.

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