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Identification of the Gene for Oral-Facial-Digital Type I Syndrome

American journal of human genetics, 2001-03, Vol.68 (3), p.569-576

2001

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A genomic rearrangement resulting in a tandem duplication is associated with split hand–split foot malformation 3 (SHFM3) at 10q24

Human molecular genetics, 2003-08, Vol.12 (16), p.1959-1971

2003

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Time and space clusters of the french-canadian MIV phenylketonuria mutation in France

American journal of human genetics, 1992-07, Vol.51 (1), p.191-196

1992

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Les années noires. La Moselle annexée par Hitler, documents et témoignages. Ed. Serpenoise, Metz, 1990

Le Pays lorrain, 1991-01, Vol.72, p.78

1991

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Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: A review

American journal of medical genetics, 1998-02, Vol.75 (4), p.389-394

1998

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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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Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia

Journal of medical genetics, 1999-04, Vol.36 (4), p.330-332

1999

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Segregation analysis in nonsyndromic holoprosencephaly

American journal of medical genetics, 1998-05, Vol.77 (2), p.139-143

1998

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Fine mapping of the human SCIDX1 locus at Xq12–13.1

Human molecular genetics, 1993-06, Vol.2 (6), p.651-654

1993

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The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52

Genomics (San Diego, Calif.), 1992-10, Vol.14 (2), p.508-510

1992

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Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus

Human genetics, 1991-02, Vol.86 (4), p.355-358

1991

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Remarks about the prognosis in case of antenatal diagnosis of gastroschisis

European journal of obstetrics & gynecology and reproductive biology, 1994-05, Vol.54 (3), p.185-190

1994

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Heredity of idiopathic haemochromatosis: A study of 106 families

Clinical genetics, 1977-04, Vol.11 (4), p.327-341

1977

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Prader–Willi syndrome and polygonosomal abnormalities in males:about a Prader–Willi/47,XYY patient

Annales de génétique, 2001, Vol.44 (1), p.1-3

2001

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Opitz GBBB syndrome: Chromosomal evidence of an X-linked form

American journal of medical genetics, 1995-10, Vol.59 (1), p.123-128

1995

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Opsismodysplasia: A new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebrae

American journal of medical genetics, 1984-09, Vol.19 (1), p.171-182

1984

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Retinoblastoma, deletion 13q14, and esterase D: Application of gene dosage effect to prenatal diagnosis

Cancer genetics and cytogenetics, 1982-01, Vol.6 (4), p.281-287

1982

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MOG1: a new susceptibility gene for Brugada syndrome

Circulation. Cardiovascular genetics, 2011-06, Vol.4 (3), p.261-268

2011

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Severe infections due to Francisella tularensis ssp. holarctica in solid organ transplant recipient: report of two cases and review of literature

BMC infectious diseases, 2019-03, Vol.19 (1), p.238-238, Article 238

2019

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Association of immune-activation and senescence markers with non-AIDS-defining comorbidities in HIV-suppressed patients

AIDS (London), 2015-10, Vol.29 (16), p.2099-2108

2015

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Tobacco, alcohol, cannabis, and illicit drug use and their association with CD4/CD8 cell count ratio in people with controlled HIV: a cross-sectional study (ANRS CO3 AQUIVIH-NA-QuAliV)

BMC infectious diseases, 2023-01, Vol.23 (1), p.16-8, Article 16

2023

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Évaluation des pratiques d’emploi accompagné : méthodologie et premières données concernant 3 dispositifs d’emploi accompagné de MESSIDOR en 2016

Pratiques en santé mentale, 2018-09, Vol.64e année (3), p.35-42

2018

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AIDS and non-AIDS severe morbidity associated with hospitalizations among HIV-infected patients in two regions with universal access to care and antiretroviral therapy, France and Brazil, 2000-2008: hospital-based cohort studies

BMC infectious diseases, 2014-05, Vol.14 (1), p.278-278, Article 278

2014

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Identification of the Gene for Oral-Facial-Digital Type I Syndrome

A genomic rearrangement resulting in a tandem duplication is associated with split hand–split foot malformation 3 (SHFM3) at 10q24

Time and space clusters of the french-canadian MIV phenylketonuria mutation in France

Les années noires. La Moselle annexée par Hitler, documents et témoignages. Ed. Serpenoise, Metz, 1990

Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: A review

Mapping of a Congenital Microcoria Locus to 13q31-q32

Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia

Segregation analysis in nonsyndromic holoprosencephaly

Fine mapping of the human SCIDX1 locus at Xq12–13.1

The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52

Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus

Remarks about the prognosis in case of antenatal diagnosis of gastroschisis

Heredity of idiopathic haemochromatosis: A study of 106 families

Prader–Willi syndrome and polygonosomal abnormalities in males:about a Prader–Willi/47,XYY patient

Opitz GBBB syndrome: Chromosomal evidence of an X-linked form

Opsismodysplasia: A new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebrae

Retinoblastoma, deletion 13q14, and esterase D: Application of gene dosage effect to prenatal diagnosis

Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite

MOG1: a new susceptibility gene for Brugada syndrome

Severe infections due to Francisella tularensis ssp. holarctica in solid organ transplant recipient: report of two cases and review of literature

Association of immune-activation and senescence markers with non-AIDS-defining comorbidities in HIV-suppressed patients

Tobacco, alcohol, cannabis, and illicit drug use and their association with CD4/CD8 cell count ratio in people with controlled HIV: a cross-sectional study (ANRS CO3 AQUIVIH-NA-QuAliV)

Chimeric oncogene regulates the EGR2 sarcoma susceptibility gene via a GGAA-microsatellite

Évaluation des pratiques d’emploi accompagné : méthodologie et premières données concernant 3 dispositifs d’emploi accompagné de MESSIDOR en 2016

AIDS and non-AIDS severe morbidity associated with hospitalizations among HIV-infected patients in two regions with universal access to care and antiretroviral therapy, France and Brazil, 2000-2008: hospital-based cohort studies

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