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Isochores and replication time zones: a perfect match

Cytogenetic and genome research, 2007-01, Vol.116 (3), p.167-172

2007

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An Isochore Transition in the NF1 Gene Region Coincides with a Switch in the Extent of Linkage Disequilibrium

American journal of human genetics, 2000-10, Vol.67 (4), p.873-880

2000

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A Comparison of the Variability Spectra of Two Genomic Loci in a European Group of Individuals Reveals Fundamental Differences Pointing to Selection or a Population Bottleneck

Annals of human genetics, 2007-05, Vol.71 (3), p.370-378

2007

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Long-range sequence composition mirrors linkage disequilibrium pattern in a 1.13 Mb region of human chromosome 22

Human molecular genetics, 2001-11, Vol.10 (24), p.2833-2839

2001

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Spinal Neurofibromatosis without Café-au-Lait Macules in Two Families with Null Mutations of the NF1 Gene

American journal of human genetics, 2001-12, Vol.69 (6), p.1395-1400

2001

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Tracing Past Human Male Movements in Northern/Eastern Africa and Western Eurasia: New Clues from Y-Chromosomal Haplogroups E-M78 and J-M12

Molecular biology and evolution, 2007-06, Vol.24 (6), p.1300-1311

2007

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A palindromic structure in the pericentromeric region of various human chromosomes

Genome research, 1996-04, Vol.6 (4), p.267-279

1996

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An RsaI polymorphism in the transcribed region of the neurofibromatosis (NF1)-gene

Human genetics, 1994-04, Vol.93 (4), p.481-482

1994

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A Candidate Gene Approach within the Susceptibility Region PCaP on 1q42.2–43 Excludes Deleterious Mutations of the PCTA-1 Gene to be Responsible for Hereditary Prostate Cancer

European urology, 2002-09, Vol.42 (3), p.301-307

2002

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Somatic NF1 mutation spectra in a family with neurofibromatosis type 1: Toward a theory of genetic modifiers

Human mutation, 2003-12, Vol.22 (6), p.423-427

2003

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Single-cell PCR performed with neurofibroma Schwann cells reveals the presence of both alleles of the neurofibromatosis type 1 (NF1) gene

Human genetics, 1995-11, Vol.96 (5), p.619-623

1995

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Genetic variability in a genomic region with long-range linkage disequilibrium reveals traces of a bottleneck in the history of the European population

Human genetics, 2005-11, Vol.118 (2), p.276-286

2005

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A small deletion and an adjacent base exchange in a potential stem-loop region of the neurofibromatosis 1 gene

Human genetics, 1991-10, Vol.87 (6), p.685-687

1991

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Toward a Survey of Somatic Mutation of the NF1 Gene in Benign Neurofibromas of Patients with Neurofibromatosis Type 1

American journal of human genetics, 2000-02, Vol.66 (2), p.393-401

2000

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An isochore transition zone in the NF1 gene region is a conserved landmark of chromosome structure and function

Genomics (San Diego, Calif.), 2005-10, Vol.86 (4), p.439-445

2005

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Characterization of an alphoid subfamily located near p-arm sequences on human chromosome 22

Chromosome research, 1999-01, Vol.7 (1), p.65-69

1999

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Germline mutations of the MSR1 gene in prostate cancer families from Germany

Human mutation, 2006-01, Vol.27 (1), p.98-102

2006

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Analysis of an alternatively spliced exon of the neurofibromatosis type 1 gene in cultured melanocytes from patients with neurofibromatosis 1

Archives of Dermatological Research, 1995-05, Vol.287 (5), p.413-416

1995

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NF1 Gene Evolution in Mammals

2008

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Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication

Human genetics, 2002-10, Vol.111 (4-5), p.465-467

2002

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RFLP detected with a 5'-bcr-gene-sequence [HGM8 provisional no. D22S11]

Nucleic acids research, 1987-02, Vol.15 (4), p.1883-1883

1987

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The size of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TSC) differs from that in fibroblasts

Human genetics, 1991-05, Vol.87 (1), p.6-10

1991

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Clonal Origin of Tumor Cells in a Plexiform Neurofibroma with LOH in NF1 Intron 38 and in Dermal Neurofibromas without LOH of the NF1 Gene

Biochemical and biophysical research communications, 1997-05, Vol.234 (2), p.346-350

1997

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SomaticNF1 mutation spectra in a family with neurofibromatosis type 1: Toward a theory of genetic modifiers

Human mutation, 2003-12, Vol.22 (6), p.423-427

2003

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Evidence for the Presence of the Second Allele of the Neurofibromatosis Type 1 Gene in Melanocytes Derived from Café au Lait Macules of NF1 Patients

Biochemical and biophysical research communications, 1997-08, Vol.237 (1), p.138-141

1997

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Isochores and replication time zones: a perfect match

An Isochore Transition in the NF1 Gene Region Coincides with a Switch in the Extent of Linkage Disequilibrium

A Comparison of the Variability Spectra of Two Genomic Loci in a European Group of Individuals Reveals Fundamental Differences Pointing to Selection or a Population Bottleneck

Long-range sequence composition mirrors linkage disequilibrium pattern in a 1.13 Mb region of human chromosome 22

Spinal Neurofibromatosis without Café-au-Lait Macules in Two Families with Null Mutations of the NF1 Gene

Tracing Past Human Male Movements in Northern/Eastern Africa and Western Eurasia: New Clues from Y-Chromosomal Haplogroups E-M78 and J-M12

A palindromic structure in the pericentromeric region of various human chromosomes

An RsaI polymorphism in the transcribed region of the neurofibromatosis (NF1)-gene

A Candidate Gene Approach within the Susceptibility Region PCaP on 1q42.2–43 Excludes Deleterious Mutations of the PCTA-1 Gene to be Responsible for Hereditary Prostate Cancer

Somatic NF1 mutation spectra in a family with neurofibromatosis type 1: Toward a theory of genetic modifiers

Single-cell PCR performed with neurofibroma Schwann cells reveals the presence of both alleles of the neurofibromatosis type 1 (NF1) gene

Genetic variability in a genomic region with long-range linkage disequilibrium reveals traces of a bottleneck in the history of the European population

A small deletion and an adjacent base exchange in a potential stem-loop region of the neurofibromatosis 1 gene

Toward a Survey of Somatic Mutation of the NF1 Gene in Benign Neurofibromas of Patients with Neurofibromatosis Type 1

An isochore transition zone in the NF1 gene region is a conserved landmark of chromosome structure and function

Characterization of an alphoid subfamily located near p-arm sequences on human chromosome 22

Germline mutations of the MSR1 gene in prostate cancer families from Germany

Analysis of an alternatively spliced exon of the neurofibromatosis type 1 gene in cultured melanocytes from patients with neurofibromatosis 1

NF1 Gene Evolution in Mammals

Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication

RFLP detected with a 5'-bcr-gene-sequence [HGM8 provisional no. D22S11]

The size of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TSC) differs from that in fibroblasts

Clonal Origin of Tumor Cells in a Plexiform Neurofibroma with LOH in NF1 Intron 38 and in Dermal Neurofibromas without LOH of the NF1 Gene

SomaticNF1 mutation spectra in a family with neurofibromatosis type 1: Toward a theory of genetic modifiers

Evidence for the Presence of the Second Allele of the Neurofibromatosis Type 1 Gene in Melanocytes Derived from Café au Lait Macules of NF1 Patients

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