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Social-Cognitive and Socio-Cultural Predictors of Hepatitis B Virus-Screening in Turkish Migrants, the Netherlands

Journal of immigrant and minority health, 2014-10, Vol.16 (5), p.811-821

2014

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Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

Nature (London), 1987-12, Vol.330 (6148), p.578-581

1987

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PREhabilitation of CAndidates for REnal Transplantation (PreCareTx) study: protocol for a hybrid type I, mixed method, randomised controlled trial

BMJ open, 2023-07, Vol.13 (7), p.e072805-e072805

2023

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An Evolutionary Rearrangement of the Xp11.3–11.23 Region in 3p21.3, a Region Frequently Deleted in a Variety of Cancers

Genomics (San Diego, Calif.), 1999-09, Vol.60 (2), p.238-240

1999

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Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes

Genes chromosomes & cancer, 2006-07, Vol.45 (7), p.676-691

2006

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Breakpoint analysis by fluorescence in situ hybridization in myelodysplastic syndromes with t(3;12)(q26;p13) and expression of EVI1

Leukemia, 2000-10, Vol.14 (10), p.1857-1858

2000

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A homozygous deletion in a small cell lung cancer cell line involving a 3p21 region with a marked instability in yeast artificial chromosomes

Cancer research (Chicago, Ill.), 1994-08, Vol.54 (15), p.4183-4187

1994

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Localization and intron usage analysis of the human CPT1B gene for muscle type carnitine palmitoyltransferase I

Biochimica et biophysica acta, 1997-05, Vol.1352 (2), p.123-128

1997

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A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer

Cancer research (Chicago, Ill.), 1992-03, Vol.52 (6), p.1536-1541

1992

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Cytogenetics of a malignant ovarian germ‐cell tumor

International journal of cancer, 1998-07, Vol.77 (2), p.217-218

1998

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FISH and array‐CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions

American journal of medical genetics. Part A, 2006-11, Vol.140A (22), p.2482-2487

2006

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PUK13 COST-EFFECTIVENESS OF INTRODUCING A DIETARY INTERVENTION FOR RENAL TRANSPLANT RECIPIENTS

Value in health, 2019-11, Vol.22, p.S915-S915

2019

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Cultural tailoring to promote hepatitis B screening in Turkish Dutch: a randomized control study

Health promotion international, 2014-12, Vol.29 (4), p.692-704

2014

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A Common Variant In Ccdc93 Decreases Ldl-C And Protects Against Myocardial Infarction By Regulating Endosomal Trafficking Of Ldl-Receptor

Atherosclerosis, 2019-08, Vol.287, p.e4-e4

2019

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Characterization of three new variant type cell lines derived from small cell carcinoma of the lung

Cancer research (Chicago, Ill.), 1985-12, Vol.45 (12), p.6024-6033

1985

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Development of a culturally tailored Internet intervention promoting hepatitis B screening in the Turkish community in the Netherlands

Health promotion international, 2012-09, Vol.27 (3), p.342-355

2012

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Prenatal diagnosis in two cases of de novo complex balanced chromosomal rearrangements. Three-year follow-up in one case

Prenatal diagnosis, 1995-05, Vol.15 (5), p.467-473

1995

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Ordering of polymorphic markers in the chromosome region 3p21

Cytogenetic and genome research, 1996-01, Vol.72 (2-3), p.225-228

1996

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Functional analysis of lung tumor suppressor activity at 3p21.3

Genes chromosomes & cancer, 2006-12, Vol.45 (12), p.1077-1093

2006

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Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22

American journal of medical genetics, 1999-09, Vol.86 (2), p.168-173

1999

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Transfection of Small Numbers of Human Endothelial Cells by Electroporation and Synthetic Amphiphiles

European journal of vascular and endovascular surgery, 1999-01, Vol.17 (1), p.9-14

1999

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Assignment of the gene coding for human cytochrome c oxidase subunit VIb to chromosome 19, band q13.1, by fluorescence in situ hybridization

Human genetics, 1991-07, Vol.87 (3), p.325-327

1991

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Ordering of markers in the pericentromeric region of chromosome 10

Human genetics, 1995-07, Vol.96 (1), p.116-118

1995

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Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13

Human genetics, 1993-06, Vol.91 (5), p.504-506

1993

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Breakpoint mapping by FISH in a Sotos patient with a constitutional translocation t(3;6)

Journal of medical genetics, 1999-04, Vol.36 (4), p.346-347

1999

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Social-Cognitive and Socio-Cultural Predictors of Hepatitis B Virus-Screening in Turkish Migrants, the Netherlands

Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

PREhabilitation of CAndidates for REnal Transplantation (PreCareTx) study: protocol for a hybrid type I, mixed method, randomised controlled trial

An Evolutionary Rearrangement of the Xp11.3–11.23 Region in 3p21.3, a Region Frequently Deleted in a Variety of Cancers

Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes

Breakpoint analysis by fluorescence in situ hybridization in myelodysplastic syndromes with t(3;12)(q26;p13) and expression of EVI1

A homozygous deletion in a small cell lung cancer cell line involving a 3p21 region with a marked instability in yeast artificial chromosomes

Localization and intron usage analysis of the human CPT1B gene for muscle type carnitine palmitoyltransferase I

A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer

Cytogenetics of a malignant ovarian germ‐cell tumor

FISH and array‐CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions

PUK13 COST-EFFECTIVENESS OF INTRODUCING A DIETARY INTERVENTION FOR RENAL TRANSPLANT RECIPIENTS

Cultural tailoring to promote hepatitis B screening in Turkish Dutch: a randomized control study

A Common Variant In Ccdc93 Decreases Ldl-C And Protects Against Myocardial Infarction By Regulating Endosomal Trafficking Of Ldl-Receptor

Characterization of three new variant type cell lines derived from small cell carcinoma of the lung

Development of a culturally tailored Internet intervention promoting hepatitis B screening in the Turkish community in the Netherlands

Prenatal diagnosis in two cases of de novo complex balanced chromosomal rearrangements. Three-year follow-up in one case

Ordering of polymorphic markers in the chromosome region 3p21

Functional analysis of lung tumor suppressor activity at 3p21.3

Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22

Transfection of Small Numbers of Human Endothelial Cells by Electroporation and Synthetic Amphiphiles

Assignment of the gene coding for human cytochrome c oxidase subunit VIb to chromosome 19, band q13.1, by fluorescence in situ hybridization

Ordering of markers in the pericentromeric region of chromosome 10

Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13

Breakpoint mapping by FISH in a Sotos patient with a constitutional translocation t(3;6)

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