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Gènes et retards de croissance intra-utérins

Archives de pédiatrie (Paris), 1998, Vol.5, p.S332-S337

Jeanpierre, M

1998

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Comparison of Autologous vs Homologous Costal Cartilage Grafts in Dorsal Augmentation Rhinoplasty: A Systematic Review and Meta-analysis

JAMA otolaryngology-- head & neck surgery, 2020-04, Vol.146 (4), p.347

2020

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Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations

Journal of neurology, 2019-12, Vol.266 (12), p.2987-2996

2019

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A Contemporary Review of the Role of Facial Prostheses in Complex Facial Reconstruction

Plastic and reconstructive surgery (1963), 2023-02, Vol.151 (2), p.288e-298e

2023

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Common SNPs of AmelogeninX (AMELX) and Dental Caries Susceptibility

Journal of dental research, 2013-05, Vol.92 (5), p.418-424

2013

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G.P.144

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.844-844

2014

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Infantile facioscapulohumeral muscular dystrophy (FSHD): A severe multi-systemic disease

European journal of paediatric neurology, 2017-06, Vol.21, p.e94-e95

2017

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A rapid method for the purification of DNA from blood

Nucleic acids research, 1987-11, Vol.15 (22), p.9611-9611

JEANPIERRE, M

1987

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L'ADN peut-il se passer de la méthylation ?

M.S. Médecine sciences, 1994, Vol.10 (3), p.351

Jeanpierre, M

1994

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Méthylation et maladies humaines: le cas du syndrome ICF

M.S. Médecine sciences, 2000, Vol.16 (1), p.105

2000

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Etablissement de l'empreinte parentale dans la lignée germinale. Conséquences pour la prise en charge en AMP

Andrologie (Lille), 2001-12, Vol.11 (4), p.209-220

2001

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Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy

Neurology, 1998-11, Vol.51 (5), p.1454-1456

1998

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An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

Human molecular genetics, 1993-06, Vol.2 (6), p.731-735

1993

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A Founder Mutation in the γ-Sarcoglycan Gene of Gypsies Possibly Predating Their Migration Out of India

Human molecular genetics, 1996-12, Vol.5 (12), p.2019-2022

1996

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Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation

Neurology, 2000-03, Vol.54 (5), p.1075-1079

2000

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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Nature genetics, 1995-06, Vol.10 (2), p.243-245

1995

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Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy

Neurology, 1997-05, Vol.48 (5), p.1227-1234

1997

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Genes and intra-uterine growth retardation

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1998-01, Vol.5 Suppl 4, p.332S-337S

Jeanpierre, M

1998

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G.P.7.11 Digenism as a cause of oculopharyngodistal myopathy

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.809-809

2007

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G.P.144: Identification of both LMNA and SMCHD1 mutations in a case with overlapping phenotypes

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.844-844

2014

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Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

Journal of medical genetics, 1997-06, Vol.34 (6), p.470-475

1997

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Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy

Annals of neurology, 2005-10, Vol.58 (4), p.569-576

2005

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M.P.4.02 Permanent muscle weakness in McArdle disease

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.859-860

2007

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Chimiothérapies dans les dernières semaines de vie : évaluation des prescriptions au centre hospitalier de Martigues

Le pharmacien hospitalier & clinicien, 2015-12, Vol.50 (4), p.380-385

2015

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Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders : rearrangements of DNA satellite II and new recurrent translocations

Leukemia, 1999-12, Vol.13 (12), p.1975-1981

1999

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Gènes et retards de croissance intra-utérins

Comparison of Autologous vs Homologous Costal Cartilage Grafts in Dorsal Augmentation Rhinoplasty: A Systematic Review and Meta-analysis

Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations

A Contemporary Review of the Role of Facial Prostheses in Complex Facial Reconstruction

Common SNPs of AmelogeninX (AMELX) and Dental Caries Susceptibility

G.P.144

Infantile facioscapulohumeral muscular dystrophy (FSHD): A severe multi-systemic disease

A rapid method for the purification of DNA from blood

L'ADN peut-il se passer de la méthylation ?

Méthylation et maladies humaines: le cas du syndrome ICF

Etablissement de l'empreinte parentale dans la lignée germinale. Conséquences pour la prise en charge en AMP

Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

A Founder Mutation in the γ-Sarcoglycan Gene of Gypsies Possibly Predating Their Migration Out of India

Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy

Genes and intra-uterine growth retardation

G.P.7.11 Digenism as a cause of oculopharyngodistal myopathy

G.P.144: Identification of both LMNA and SMCHD1 mutations in a case with overlapping phenotypes

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy

M.P.4.02 Permanent muscle weakness in McArdle disease

Chimiothérapies dans les dernières semaines de vie : évaluation des prescriptions au centre hospitalier de Martigues

Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders : rearrangements of DNA satellite II and new recurrent translocations

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