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Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

Nature genetics, 1997-06, Vol.16 (2), p.184-187

1997

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Genetic Linkage of a Polymorphism in the Type II Procollagen Gene (COL2A1) to Primary Osteoarthritis Associated with Mild Chondrodysplasia

The New England journal of medicine, 1990-02, Vol.322 (8), p.526-530

1990

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Mutations in the Cartilage Oligomeric Matrix Protein (COMP) Gene in Pseudoachondroplasia and Multiple Epiphyseal Dysplasia

Annals of the New York Academy of Sciences, 1996-06, Vol.785 (1), p.188-194

1996

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Application of a numerical model for simulating water flow, isotope transport, and heat transfer in the unsaturated zone

Journal of hydrology (Amsterdam), 1995-09, Vol.171 (1), p.143-163

1995

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A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7

Nature (London), 1985-11, Vol.318 (6044), p.380-382

1985

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Recent Trend for Environmental Compliance Provides New Opportunities for Land and Water Use at Brownfields and Other Contaminated Sites

Natural resources journal, 2001-10, Vol.41 (4), p.919-943

2001

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Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease Spectrum

American journal of human genetics, 1998-02, Vol.62 (2), p.311-319

1998

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Stop Codon in the Procollagen II Gene (COL2A1) in a Family with the Stickler Syndrome (Arthro-Ophthalmopathy)

Proceedings of the National Academy of Sciences - PNAS, 1991-08, Vol.88 (15), p.6624-6627

1991

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Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene

The Journal of clinical investigation, 1992-09, Vol.90 (3), p.1032-1036

1992

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Human type VII collagen : genetic linkage of the gene (COL7AI) on chromosome 3 to dominant dystrophic epidermolysis bullosa

American journal of human genetics, 1991-10, Vol.49 (4), p.797-803

1991

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Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils

The Journal of clinical investigation, 1992-03, Vol.89 (3), p.974-980

1992

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A second mutation in the type II procollagen gene (COL2A1) causing Stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon

American journal of human genetics, 1993, Vol.52 (1), p.39-45

1993

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Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA Pooling

Human molecular genetics, 1997-05, Vol.6 (5), p.689-694

1997

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Mixed Hematopoietic Chimerism Following Bone Marrow Transplantation for Hematologic Malignancies

Blood, 1987-11, Vol.70 (5), p.1331-1337

1987

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Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19

American journal of human genetics, 1994, Vol.54 (1), p.3-10

1994

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Stickler syndrome. A mutation in the nonhelical 3' end of type II procollagen gene

Archives of ophthalmology (1960), 1995-11, Vol.113 (11), p.1454

1995

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Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1)

Human genetics, 1993-11, Vol.92 (5), p.499-505

1993

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Mapping of epidermolysis bullosa simplex mutation to chromosome 12

American journal of human genetics, 1991-11, Vol.49 (5), p.978-984

1991

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Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia

Human mutation, 1998, Vol.11 (S1), p.S10-S17

1998

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Localization of the Krabbe disease gene (GALC) on chromosome 14 by multipoint linkage analysis

American journal of human genetics, 1993-12, Vol.53 (6), p.1250-1255

1993

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Use of Highly Polymorphic DNA Probes for Genotypic Analysis Following Bone Marrow Transplantation

Blood, 1986-08, Vol.68 (2), p.378-385

1986

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Krabbe disease locus mapped to chromosome 14 by genetic linkage

American journal of human genetics, 1990-07, Vol.47 (1), p.37-44

1990

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Use of DNA restriction fragment length polymorphisms to document marrow engraftment and mixed hematopoietic chimerism following bone marrow transplantation

Transplantation, 1987, Vol.43 (3), p.399

1987

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Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene cluster

The Journal of clinical investigation, 1993-01, Vol.91 (1), p.357-361

1993

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Vadose Zone Characterization of Low-Permeability Sediments Using Field Permeameters

Ground water monitoring & remediation, 1988-06, Vol.8 (2), p.59-66

1988

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Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

Genetic Linkage of a Polymorphism in the Type II Procollagen Gene (COL2A1) to Primary Osteoarthritis Associated with Mild Chondrodysplasia

Mutations in the Cartilage Oligomeric Matrix Protein (COMP) Gene in Pseudoachondroplasia and Multiple Epiphyseal Dysplasia

Application of a numerical model for simulating water flow, isotope transport, and heat transfer in the unsaturated zone

A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7

Recent Trend for Environmental Compliance Provides New Opportunities for Land and Water Use at Brownfields and Other Contaminated Sites

Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease Spectrum

Stop Codon in the Procollagen II Gene (COL2A1) in a Family with the Stickler Syndrome (Arthro-Ophthalmopathy)

Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene

Human type VII collagen : genetic linkage of the gene (COL7AI) on chromosome 3 to dominant dystrophic epidermolysis bullosa

Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils

A second mutation in the type II procollagen gene (COL2A1) causing Stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon

Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA Pooling

Mixed Hematopoietic Chimerism Following Bone Marrow Transplantation for Hematologic Malignancies

Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19

Stickler syndrome. A mutation in the nonhelical 3' end of type II procollagen gene

Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1)

Mapping of epidermolysis bullosa simplex mutation to chromosome 12

Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia

Localization of the Krabbe disease gene (GALC) on chromosome 14 by multipoint linkage analysis

Use of Highly Polymorphic DNA Probes for Genotypic Analysis Following Bone Marrow Transplantation

Krabbe disease locus mapped to chromosome 14 by genetic linkage

Use of DNA restriction fragment length polymorphisms to document marrow engraftment and mixed hematopoietic chimerism following bone marrow transplantation

Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene cluster

Vadose Zone Characterization of Low-Permeability Sediments Using Field Permeameters

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