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The early-onset torsion dystonia gene ( DYT1 ) encodes an ATP-binding protein

Nature genetics, 1997-09, Vol.17 (1), p.40-48

1997

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Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury ( T ) gene family

Nature genetics, 1997-01, Vol.15 (1), p.21-29

1997

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Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Nature (London), 1992-02, Vol.355 (6360), p.545-546

1992

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Isolation of genes from complex sources of mammalian genomic DNA using exon amplification

Nature genetics, 1994-01, Vol.6 (1), p.98-105

1994

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Inactivating Mutations in an SH2 Domain-Encoding Gene in X-Linked Lymphoproliferative Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1998-11, Vol.95 (23), p.13765-13770

1998

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Isolation of a novel gene underlying batten disease, CLN3

Cell, 1995-01, Vol.82 (6), p.949-957

1995

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Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

Cell, 1990-02, Vol.60 (3), p.509-520

1990

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Exon Amplification: A Strategy to Isolate Mammalian Genes Based on RNA Splicing

Proceedings of the National Academy of Sciences - PNAS, 1991-05, Vol.88 (9), p.4005-4009

1991

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Identification and characterization of novel human transcripts embedded within HMGA2 in t(12;14)(q15;q24.1) uterine leiomyoma

Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis, 2006-12, Vol.602 (1), p.43-53

2006

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An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

Cell, 1990-06, Vol.61 (7), p.1257-1269

1990

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Alternative Splicing and Genomic Structure of the Wilms Tumor Gene WT1

Proceedings of the National Academy of Sciences - PNAS, 1991-11, Vol.88 (21), p.9618-9622

1991

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

Cell, 1993-03, Vol.72 (6), p.971-983

1993

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p16 Alterations and deletion mapping of 9p21-p22 in malignant mesothelioma

Cancer research (Chicago, Ill.), 1994-11, Vol.54 (21), p.5547-5551

1994

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

Cell, 1993-03, Vol.72 (5), p.791-800

1993

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Expression of the Wilms' tumor gene WT1 in the murine urogenital system

Genes & development, 1991-08, Vol.5 (8), p.1345-1356

1991

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p619, a giant protein related to the chromosome condensation regulator RCC1, stimulates guanine nucleotide exchange on ARF1 and Rab proteins

The EMBO journal, 1996-08, Vol.15 (16), p.4262-4273

1996

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Role of Rel-related factors in control of c-myc gene transcription in receptor-mediated apoptosis of the murine B cell WEHI 231 line

The Journal of experimental medicine, 1995-03, Vol.181 (3), p.1169-1177

1995

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Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development

Molecular and Cellular Biology, 1991-03, Vol.11 (3), p.1707-1712

1991

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Interaction of an NF-κB-Like Factor with a Site Upstream of the C-MYC Promoter

Proceedings of the National Academy of Sciences - PNAS, 1990-06, Vol.87 (12), p.4727-4731

1990

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MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p

Human molecular genetics, 1994-10, Vol.3 (10), p.1841-1845

1994

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Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium

Genome research, 1997-05, Vol.7 (5), p.483-494

1997

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hREC2, a RAD51-like Gene, is Disrupted by t(12;14)(q15;q24.1) in a Uterine Leiomyoma

Cancer genetics and cytogenetics, 1999-11, Vol.115 (1), p.56-61

1999

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[6] Gene identification by exon amplification

Methods in Enzymology, 1999, Vol.303, p.83-99

1999

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Genomic organization and transcriptional units at the myotonic dystrophy locus

Genomics (San Diego, Calif.), 1993-12, Vol.18 (3), p.673-679

1993

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The early-onset torsion dystonia gene ( DYT1 ) encodes an ATP-binding protein

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury ( T ) gene family

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification

Inactivating Mutations in an SH2 Domain-Encoding Gene in X-Linked Lymphoproliferative Syndrome

Isolation of a novel gene underlying batten disease, CLN3

Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

Exon Amplification: A Strategy to Isolate Mammalian Genes Based on RNA Splicing

Identification and characterization of novel human transcripts embedded within HMGA2 in t(12;14)(q15;q24.1) uterine leiomyoma

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

Alternative Splicing and Genomic Structure of the Wilms Tumor Gene WT1

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

p16 Alterations and deletion mapping of 9p21-p22 in malignant mesothelioma

A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

Expression of the Wilms' tumor gene WT1 in the murine urogenital system

p619, a giant protein related to the chromosome condensation regulator RCC1, stimulates guanine nucleotide exchange on ARF1 and Rab proteins

Role of Rel-related factors in control of c-myc gene transcription in receptor-mediated apoptosis of the murine B cell WEHI 231 line

Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development

Interaction of an NF-κB-Like Factor with a Site Upstream of the C-MYC Promoter

MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p

Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium

hREC2, a RAD51-like Gene, is Disrupted by t(12;14)(q15;q24.1) in a Uterine Leiomyoma

[6] Gene identification by exon amplification

Genomic organization and transcriptional units at the myotonic dystrophy locus

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