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MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia

Genomics (San Diego, Calif.), 2000-07, Vol.67 (1), p.54-68

2000

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A gene ( PEX ) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets

Nature genetics, 1995-10, Vol.11 (2), p.130-136

1995

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Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP)

Human molecular genetics, 1997-04, Vol.6 (4), p.539-549

1997

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Génétique du rachitisme hypophosphatémique familial: intérét pour le clinicien

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1996-08, Vol.3 (8), p.834-834

Oudet, C.

1996

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Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes

American journal of human genetics, 1993-02, Vol.52 (2), p.297-304

1993

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A second family with XLRH displays the mutation S244L in the CLCN5 gene

Human genetics, 1997-06, Vol.99 (6), p.781-784

1997

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Striking founder effect for the fragile X syndrome in Finland

European journal of human genetics : EJHG, 1993, Vol.1 (3), p.181-189

1993

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An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene

Human genetics, 1990-02, Vol.84 (3), p.283-285

1990

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M13 endopeptidases: New conserved motifs correlated with structure, and simultaneous phylogenetic occurrence of PHEX and the bony fish

Proteins, structure, function, and bioinformatics, 2002-06, Vol.47 (4), p.481-488

2002

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Strong founder effect for the fragile X syndrome in Sweden

European journal of human genetics : EJHG, 1994, Vol.2 (2), p.103-109

1994

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Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets

Genome research, 1997-06, Vol.7 (6), p.573

1997

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Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2

American journal of human genetics, 1992-05, Vol.50 (5), p.981-987

1992

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Effects of structure on the tensile, creep and fatigue properties of polyester fibres

Journal of materials science, 1987-12, Vol.22 (12), p.4292-4298

1987

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Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2)

Human genetics, 1994-03, Vol.93 (3), p.291-294

1994

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Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues

European journal of human genetics : EJHG, 1999-07, Vol.7 (5), p.615-619

1999

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An informative polymorphism detectable by polymerase chain reaction at the 3' end of dystrophin gene

Human genetics, 1990-10, Vol.85 (6), p.677-677

1990

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Two hot spots of recombination in the DMD gene correlate with the deletion prone regions

Human molecular genetics, 1992-11, Vol.1 (8), p.599-603

1992

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A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia : Evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets

The journal of clinical endocrinology and metabolism, 1998-10, Vol.83 (10), p.3459-3462

1998

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FRAXAC2 instability

Nature genetics, 1994-06, Vol.7 (2), p.122-122

1994

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FRAXAC2 instability

Nature genetics, 1994-06, Vol.7 (2), p.122; author reply 123-123

1994

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Time-Dependent Effects of a Functional'-Type Orthopedic Appliance on the Rat Mandible Growth

Chronobiology international, 1984, Vol.1 (1), p.51-57

1984

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An experimental orthopedic treatment of the rat mandible using a functional appliance alters the fibre and myosin types in masticatory muscles

Reproduction, nutrition, développement, 1988, Vol.28 (3B), p.795

1988

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An electron microscopy study of the polyethylene fibres

Journal of materials science letters, 1991-09, Vol.10 (18), p.1061-1065

1991

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The gene for X-linked hypophosphataemic rickets maps to a 200-300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)

Human genetics, 1996-03, Vol.97 (3), p.345-352

1996

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Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination

American journal of human genetics, 1991-08, Vol.49 (2), p.311-319

1991

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MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia

A gene ( PEX ) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets

Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP)

Génétique du rachitisme hypophosphatémique familial: intérét pour le clinicien

Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes

A second family with XLRH displays the mutation S244L in the CLCN5 gene

Striking founder effect for the fragile X syndrome in Finland

An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene

M13 endopeptidases: New conserved motifs correlated with structure, and simultaneous phylogenetic occurrence of PHEX and the bony fish

Strong founder effect for the fragile X syndrome in Sweden

Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets

Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2

Effects of structure on the tensile, creep and fatigue properties of polyester fibres

Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2)

Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues

An informative polymorphism detectable by polymerase chain reaction at the 3' end of dystrophin gene

Two hot spots of recombination in the DMD gene correlate with the deletion prone regions

A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia : Evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets

FRAXAC2 instability

FRAXAC2 instability

Time-Dependent Effects of a Functional'-Type Orthopedic Appliance on the Rat Mandible Growth

An experimental orthopedic treatment of the rat mandible using a functional appliance alters the fibre and myosin types in masticatory muscles

An electron microscopy study of the polyethylene fibres

The gene for X-linked hypophosphataemic rickets maps to a 200-300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)

Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination

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