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Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen

Nature genetics, 1994-07, Vol.7 (3), p.429-432

1994

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Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

Journal of medical genetics, 1997-03, Vol.34 (3), p.177-183

1997

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Predisposing Gene for Early-Onset Prostate Cancer, Localized on Chromosome 1q42.2-43

American journal of human genetics, 1998-06, Vol.62 (6), p.1416-1424

1998

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Mapping of a gene for long QT syndrome to chromosome 4q25-27

American journal of human genetics, 1995-11, Vol.57 (5), p.1114-1122

1995

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The Hereditary Pancreatitis Gene Maps to Long Arm of Chromosome 7

Human molecular genetics, 1996-04, Vol.5 (4), p.549-554

1996

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Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa

Journal of medical genetics, 1994-04, Vol.31 (4), p.342-343

1994

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Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)

Journal of medical genetics, 1990-10, Vol.27 (10), p.603-613

1990

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In vivo developmental modifications of the expression of genes encoding muscle-specific enzymes in rat

The Journal of biological chemistry, 1986-08, Vol.261 (22), p.10271-10276

1986

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Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

Human molecular genetics, 1993-09, Vol.2 (9), p.1423-1428

1993

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Hétérogénéité génétique des retards mentaux non spécifiques liés au chromosome X: étude clinique et génétique de deux familles

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1996-09, Vol.3 (9), p.923-923

1996

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Crystallinity and mechanical properties of PP-homopolymers as influenced by molecular structure and nucleation

Journal of applied polymer science, 1996-07, Vol.61 (4), p.649-657

1996

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Localisation en Xp22.33-pter d'un syndrome neurodégénératif familial récessif lié au chromosome X, caractérisé par une ataxie congénitale, une épilepsie myoclonique progressive et une rétinopathie maculaire

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1996-09, Vol.3 (9), p.930-930

1996

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Polyxanthylic acid and its complexes

European journal of biochemistry, 1973-05, Vol.35 (1), p.95-105

1973

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Mapping of a Congenital Microcoria Locus to 13q31-q32

American journal of human genetics, 1998-05, Vol.62 (5), p.1117-1122

1998

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Thermal dissociation in several stages of polyxanthylic acid

Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles, 1971-06, Vol.272 (23), p.2965

1971

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An improved and easy technique for polyamine determination in biological samples : Application to cell-free system from hypertrophied rat heart

Journal of chromatography, 1979-04, Vol.162 (4), p.547-559

1979

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A gene for dominant nonspecific X-linked mental retardation is located in Xq28

American journal of human genetics, 1997-04, Vol.60 (4), p.903-909

1997

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Molecular genetics and polycystic kidney diseases

Advances in nephrology from the Necker Hospital, 1989, Vol.18, p.3

1989

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Independent expression of cyclic AMP dependent protein kinases related to cyclic nucleotide systems, during triiodothyronine induced cardiac hypertrophy

Life sciences (1973), 1980-01, Vol.27 (5), p.387-394

1980

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A continuous high molecular weight base-paired structure is not an absolute requirement for a potential polynucleotide inducer of interferon

FEBS letters, 1977-04, Vol.76 (2), p.159-165

1977

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Ten novel mutations in the HEXA gene in non-Jewish Tay — Sachs patients

Human molecular genetics, 1993-01, Vol.2 (1), p.61-67

1993

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Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency

Comptes rendus de l'Académie des sciences, Série III, Sciences de la vie, 1994-01, Vol.317 (1), p.70

1994

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Ten novel mutations in the HEXA gene in non-Jewish Tay-Sachs patients

Human molecular genetics, 1993-04, Vol.2 (4), p.496-496

1993

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Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markers

Genomics (San Diego, Calif.), 1992-05, Vol.13 (1), p.152-158

1992

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X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pter

American journal of medical genetics, 1996-07, Vol.64 (1), p.69-72

1996

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Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

Predisposing Gene for Early-Onset Prostate Cancer, Localized on Chromosome 1q42.2-43

Mapping of a gene for long QT syndrome to chromosome 4q25-27

The Hereditary Pancreatitis Gene Maps to Long Arm of Chromosome 7

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa

Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)

In vivo developmental modifications of the expression of genes encoding muscle-specific enzymes in rat

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

Hétérogénéité génétique des retards mentaux non spécifiques liés au chromosome X: étude clinique et génétique de deux familles

Crystallinity and mechanical properties of PP-homopolymers as influenced by molecular structure and nucleation

Localisation en Xp22.33-pter d'un syndrome neurodégénératif familial récessif lié au chromosome X, caractérisé par une ataxie congénitale, une épilepsie myoclonique progressive et une rétinopathie maculaire

Polyxanthylic acid and its complexes

Mapping of a Congenital Microcoria Locus to 13q31-q32

Thermal dissociation in several stages of polyxanthylic acid

An improved and easy technique for polyamine determination in biological samples : Application to cell-free system from hypertrophied rat heart

A gene for dominant nonspecific X-linked mental retardation is located in Xq28

Molecular genetics and polycystic kidney diseases

Independent expression of cyclic AMP dependent protein kinases related to cyclic nucleotide systems, during triiodothyronine induced cardiac hypertrophy

A continuous high molecular weight base-paired structure is not an absolute requirement for a potential polynucleotide inducer of interferon

Ten novel mutations in the HEXA gene in non-Jewish Tay — Sachs patients

Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency

Ten novel mutations in the HEXA gene in non-Jewish Tay-Sachs patients

Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markers

X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pter

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