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Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2

American journal of human genetics, 2000-04, Vol.66 (4), p.1432-1436

2000

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Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

Nature genetics, 1995-11, Vol.11 (3), p.341-343

1995

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Fifty-Four New Gene-Based Canine Microsatellite Markers

The Journal of heredity, 2005-11, Vol.96 (7), p.843-846

2005

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Mammalian SNM1 is required for genome stability

Molecular genetics and metabolism, 2008-05, Vol.94 (1), p.38-45

2008

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Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

American journal of human genetics, 2000-05, Vol.66 (5), p.1540-1551

2000

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Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

Journal of cardiac failure, 2001-09, Vol.7 (3), p.249-256

2001

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Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

American journal of human genetics, 2006-12, Vol.79 (6), p.1030-1039

2006

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Cloning and Characterization of a Human cDNA (INPPL1) Sharing Homology with Inositol Polyphosphate Phosphatases

Genomics (San Diego, Calif.), 1995-09, Vol.29 (1), p.285-287

1995

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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

Nature genetics, 1993-06, Vol.4 (2), p.202-205

1993

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Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure

Somatic cell and molecular genetics, 1996-03, Vol.22 (2), p.151-157

1996

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Complementation group assignments in Fanconi anemia fibroblast cell lines from North America

Somatic cell and molecular genetics, 1997-01, Vol.23 (1), p.1-7

1997

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Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome

Mammalian genome, 1999-04, Vol.10 (4), p.381-384

1999

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Cephalopod myocardial receptors: pharmacological studies on the isolated heart of Sepia officinalis (L.)

Experientia, 1987-05, Vol.43 (5), p.511-525

1987

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Topo IIIα and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

Cytogenetic and genome research, 2009-09, Vol.125 (3), p.165-175

2009

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Monoaminergic-peptidergic interactions in neuroregulatory control of the cephalic aorta in Sepia officinalis L. (cephalopoda)

Comparative biochemistry and physiology. C, Comparative pharmacology, 1991, Vol.99 (3), p.421-429

1991

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The electrocardiogram of Sepia officinalis L. (cephalopoda: coleoida) and its modulation by neuropeptides of the FMRFamide group

Comparative biochemistry and physiology. C, Comparative pharmacology, 1992-10, Vol.103 (2), p.399-402

1992

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Topo IIIa and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

Cytogenetic and genome research, 2009-09, Vol.125 (3), p.165-175

2009

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Topo III[alpha] and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

Cytogenetic and genome research, 2009-09, Vol.125 (3), p.165

2009

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A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation

The American heart journal, 2002-12, Vol.144 (6), p.1081-1086

2002

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Fanconi anemia cells have a normal gene structure for topoisomerase I

Human genetics, 1994-05, Vol.93 (5), p.583-586

1994

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Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia

Blood, 2003-07, Vol.102 (1), p.7-16

2003

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A European view on forensic expertise and counter-expertise

Criminal law forum, 2000-01, Vol.11 (3), p.375-392

2000

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Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

Journal of cardiac failure, 2002-02, Vol.8 (1), p.28-32

2002

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Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents

Cytogenetic and genome research, 2009, Vol.125 (3), p.165

2009

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Fanconi anemia cells have a normal gene structure for topoisomerase I

Human genetics, 1994-05, Vol.93 (5), p.583-586

1994

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Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

Fifty-Four New Gene-Based Canine Microsatellite Markers

Mammalian SNM1 is required for genome stability

Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

Cloning and Characterization of a Human cDNA (INPPL1) Sharing Homology with Inositol Polyphosphate Phosphatases

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure

Complementation group assignments in Fanconi anemia fibroblast cell lines from North America

Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome

Cephalopod myocardial receptors: pharmacological studies on the isolated heart of Sepia officinalis (L.)

Topo IIIα and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

Monoaminergic-peptidergic interactions in neuroregulatory control of the cephalic aorta in Sepia officinalis L. (cephalopoda)

The electrocardiogram of Sepia officinalis L. (cephalopoda: coleoida) and its modulation by neuropeptides of the FMRFamide group

Topo IIIa and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

Topo III[alpha] and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation

Fanconi anemia cells have a normal gene structure for topoisomerase I

Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia

A European view on forensic expertise and counter-expertise

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents

Fanconi anemia cells have a normal gene structure for topoisomerase I

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