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Accuracy of lactase gene C/T-13910 polymorphism and hydrogen breath test in a gastroenterology outpatient clinic: a retrospective study

Orvosi hetilap, 2016-06, Vol.157 (25), p.1007

2016

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Association of some rare haplotypes and genotype combinations in the MDR1 gene with childhood acute lymphoblastic leukaemia

Leukemia research, 2008-08, Vol.32 (8), p.1214-1220

2008

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Rapid detection of cystic fibrosis transmembrane conductance regulator gene IVS8 5T variant by real-time PCR

Clinical chemistry (Baltimore, Md.), 2004-10, Vol.50 (10), p.1837-1839

2004

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The role of ABC-transporter gene polymorphisms in chemotherapy induced immunosuppression, a retrospective study in childhood acute lymphoblastic leukaemia

Cellular immunology, 2006-12, Vol.244 (2), p.121-124

2006

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Laktózintolerancia: a laktázgén C/T-13910 polimorfizmusának és a hidrogénkilégzési teszt pontosságának retrospektív kiértékelése gasztroenterológiai szakrendelésen

Orvosi hetilap, 2016-06, Vol.157 (25), p.1007-1012

2016

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Mutations causing biotinidase deficiency in children ascertained by newborn screening in Western Hungary

Molecular genetics and metabolism, 2007-03, Vol.90 (3), p.345-348

2007

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Molecular mechanisms in the antiproliferative action of quercetin

Life sciences (1973), 1997, Vol.60 (24), p.2157-2163

1997

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Sequence alterations can mask each other's presence during screening with SSCP or heteroduplex analysis : BRCA genes as examples

BioTechniques, 2000-07, Vol.29 (1), p.94-98

2000

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Prevalence of founder BRCA1 and BRCA2 mutations among breast and ovarian cancer patients in Hungary

International journal of cancer, 2000-06, Vol.86 (5), p.737-740

2000

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Haplotype and Phenotype Analysis of Nine Recurrent BRCA2 Mutations in 111 Families: Results of an International Study

American journal of human genetics, 1998-06, Vol.62 (6), p.1381-1388

1998

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High frequency of germ-line BRCA2 mutations among hungarian male breast cancer patients without family history

Cancer research (Chicago, Ill.), 1999-03, Vol.59 (5), p.995-998

1999

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Sequence Alterations Can Mask Each Other's Presence during Screening with SSCP or Heteroduplex Analysis

BioTechniques, 2000-07, Vol.29 (1), p.94-98

2000

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Molecular mechanisms in the antiproliferative action of taxol and tiazofurin

Anticancer research, 1996-09, Vol.16 (5A), p.2469

1996

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Strong founder effects in BRCA1 mutation carrier breast cancer patients from Latvia

Human mutation, 1999, Vol.14 (1), p.92-92

1999

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Prevalence of founderBRCA1 andBRCA2 mutations among breast and ovarian cancer patients in hungary

International journal of cancer, 2000-06, Vol.86 (5), p.737-740

2000

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Rapid detection of sex chromosomal aneuploidies by QF-PCR: application in 200 men with severe oligozoospermia or azoospermia

Genetic testing, 2007-06, Vol.11 (2), p.139-145

2007

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Regulation of the signal transduction program by drugs

Advances in enzyme regulation, 1997, Vol.37, p.35-55

1997

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Accuracy of lactase gene C/T-13910 polymorphism and hydrogen breath test in a gastroenterology outpatient clinic: a retrospective study

Association of some rare haplotypes and genotype combinations in the MDR1 gene with childhood acute lymphoblastic leukaemia

Rapid detection of cystic fibrosis transmembrane conductance regulator gene IVS8 5T variant by real-time PCR

The role of ABC-transporter gene polymorphisms in chemotherapy induced immunosuppression, a retrospective study in childhood acute lymphoblastic leukaemia

Laktózintolerancia: a laktázgén C/T-13910 polimorfizmusának és a hidrogénkilégzési teszt pontosságának retrospektív kiértékelése gasztroenterológiai szakrendelésen

Mutations causing biotinidase deficiency in children ascertained by newborn screening in Western Hungary

Molecular mechanisms in the antiproliferative action of quercetin

Sequence alterations can mask each other's presence during screening with SSCP or heteroduplex analysis : BRCA genes as examples

Prevalence of founder BRCA1 and BRCA2 mutations among breast and ovarian cancer patients in Hungary

Haplotype and Phenotype Analysis of Nine Recurrent BRCA2 Mutations in 111 Families: Results of an International Study

High frequency of germ-line BRCA2 mutations among hungarian male breast cancer patients without family history

Sequence Alterations Can Mask Each Other's Presence during Screening with SSCP or Heteroduplex Analysis

Molecular mechanisms in the antiproliferative action of taxol and tiazofurin

Strong founder effects in BRCA1 mutation carrier breast cancer patients from Latvia

Prevalence of founderBRCA1 andBRCA2 mutations among breast and ovarian cancer patients in hungary

Rapid detection of sex chromosomal aneuploidies by QF-PCR: application in 200 men with severe oligozoospermia or azoospermia

Regulation of the signal transduction program by drugs

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