Suchergebnisse - "Borun, Pawel"

1

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11gene in patients with Peutz-Jeghers syndrome

von: Borun, Pawel

2013, in: BMC medical genetics

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2

Absence of the RET+3:T allele in the MTC patients

von: Borun Pawel

2012, in: Hereditary Cancer in Clinical Practice

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3

Absence of the RET+3:T allele in the MTC patients

von: Borun, Pawel

2012, in: Hereditary cancer in clinical practice

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4

A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome

von: Boruń Paweł

2012, in: Hereditary Cancer in Clinical Practice

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5

Comparative-high resolution melting: a novel method of simultaneous screening for small mutations and copy number variations

von: Borun, Pawel

2013, in: Human genetics

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6

A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome

von: Boruń, Paweł

2012, in: Hereditary cancer in clinical practice

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7

Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz–Jeghers syndrome

von: Borun, Pawel

2015, in: Familial cancer

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8

Rapid Detection Method for the Four Most Common CHEK2 Mutations Based on Melting Profile Analysis

von: Borun, Pawel

2015, in: Molecular diagnosis & therapy

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9

Familial adenomatous polyposis of the colon

von: Plawski, Andrzej

2013, in: Hereditary cancer in clinical practice

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10

Influence of lactose intolerance on colorectal cancer incidence in the Polish population

von: Andrzej, Plawski

2015, in: Hereditary cancer in clinical practice

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11

Hamartomatous polyposis syndromes

von: Stojcev, Zoran

2013, in: Hereditary cancer in clinical practice

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12

A Simple Method for TPMT and ITPA Genotyping Using Multiplex HRMA for Patients Treated with Thiopurine Drugs

von: Skrzypczak-Zielinska, Marzena

2016, in: Molecular diagnosis & therapy

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13

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland

von: Plawski, Andrzej

2012, in: Hereditary cancer in clinical practice

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14

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland

von: Plawski Andrzej

2012, in: Hereditary Cancer in Clinical Practice

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15

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015

von: Thompson, Ella R.

2017, in: Hereditary cancer in clinical practice

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