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UroVysion Compared with Cytology and Quantitative Cytology in the Surveillance of Non–Muscle-Invasive Bladder Cancer

European urology, 2007-05, Vol.51 (5), p.1275-1280

2007

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p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation

American journal of human genetics, 2001-09, Vol.69 (3), p.481-492

2001

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A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification

Human molecular genetics, 2002-11, Vol.11 (23), p.2867-2875

2002

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Deficiency of Either P-Glycoprotein or Breast Cancer Resistance Protein Protect against Acute Kidney Injury

Cell transplantation, 2010-01, Vol.19 (9), p.1195-1208

2010

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Retracted: Deficiency of Either P-Glycoprotein or Breast Cancer Resistance Protein Protect against Acute Kidney Injury

Cell transplantation, 2010-09, Vol.19 (9), p.1195-1208

2010

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Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families

Pediatric nephrology (Berlin, West), 1996-08, Vol.10 (4), p.403-407

1996

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Urovysion compared with cytology and quantitative cytology in the surveillance of non-muscle-invasive bladder cancer. Commentary

European urology, 2007, Vol.51 (5), p.1275-1280

2007

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Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes

Human genetics, 1991-05, Vol.87 (1), p.45-48

1991

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High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization

American journal of human genetics, 2002-05, Vol.70 (5), p.1269-1276

2002

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Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma

Genes chromosomes & cancer, 2013-01, Vol.52 (1), p.11-23

2013

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CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation

Human genetics, 2010-09, Vol.128 (3), p.281-291

2010

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A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene

Human molecular genetics, 1995-11, Vol.4 (11), p.2145-2150

1995

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ICF syndrome : a new case and review of the literature

Human genetics, 1994-09, Vol.94 (3), p.240-246

1994

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Genomic organization, chromosomal localization, and 5' upstream region of the human DC-STAMP gene

Immunogenetics (New York), 2001-03, Vol.53 (2), p.145-149

2001

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Assignment of the human adipocyte fatty acid-binding protein gene (FABP4) to chromosome 8q21 using somatic cell hybrid and fluorescence in situ hybridization techniques

Genomics (San Diego, Calif.), 1997-02, Vol.40 (1), p.207-209

1997

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cDNA Cloning and Chromosomal Localization of the Genes Encoding the α- and β-Subunits of Human Rab Geranylgeranyl Transferase: The 3′ End of the α-Subunit Gene Overlaps with the Transglutaminase 1 Gene Promoter

Genomics (San Diego, Calif.), 1996-12, Vol.38 (2), p.133-140

1996

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Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes

Human genetics, 1990-11, Vol.86 (1), p.76-78

1990

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Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma

Cancer genetics and cytogenetics, 2009-08, Vol.193 (1), p.54-62

2009

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UroVysion Compared with Cytology and Quantitative Cytology in the Surveillance of Non–Muscle-Invasive Bladder Cancer

p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation

A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification

Deficiency of Either P-Glycoprotein or Breast Cancer Resistance Protein Protect against Acute Kidney Injury

Retracted: Deficiency of Either P-Glycoprotein or Breast Cancer Resistance Protein Protect against Acute Kidney Injury

Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families

Urovysion compared with cytology and quantitative cytology in the surveillance of non-muscle-invasive bladder cancer. Commentary

Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes

High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization

Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma

CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation

A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene

ICF syndrome : a new case and review of the literature

Genomic organization, chromosomal localization, and 5' upstream region of the human DC-STAMP gene

Assignment of the human adipocyte fatty acid-binding protein gene (FABP4) to chromosome 8q21 using somatic cell hybrid and fluorescence in situ hybridization techniques

cDNA Cloning and Chromosomal Localization of the Genes Encoding the α- and β-Subunits of Human Rab Geranylgeranyl Transferase: The 3′ End of the α-Subunit Gene Overlaps with the Transglutaminase 1 Gene Promoter

Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes

Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma

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