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Bubbles slipping along a crenelated wall

Europhysics letters, 2016-09, Vol.115 (6), p.64005-64005

2016

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Viscous mechanism for Leidenfrost propulsion on a ratchet

Europhysics letters, 2011-12, Vol.96 (5), p.58001

2011

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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

Journal of medical genetics, 2006-11, Vol.43 (11), p.843-849

2006

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Holes and cracks in rigid foam films

Journal of fluid mechanics, 2015-07, Vol.774, p.074302; 226101; 054501; 094501-074302; 226101; 054501; 094501, Article R3

2015

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Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patients

European journal of endocrinology, 2014-05, Vol.170 (5), p.677-684

2014

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Three‐dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasia

Ultrasound in obstetrics & gynecology, 2013-08, Vol.42 (2), p.161-168

2013

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Genotype-phenotype correlation in hereditary multiple exostoses

Journal of medical genetics, 2001-07, Vol.38 (7), p.430-434

2001

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Lamin a Truncation in Hutchinson-Gilford Progeria

Science (American Association for the Advancement of Science), 2003-06, Vol.300 (5628), p.2055-2055

2003

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Spectrum of NSD1 mutations in Sotos and Weaver syndromes

Journal of medical genetics, 2003-06, Vol.40 (6), p.436-440

2003

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Slicing softly with shear

Physical review letters, 2012-12, Vol.109 (24), p.244301-244301, Article 244301

2012

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Level-set simulations of a 2D topological rearrangement in a bubble assembly: effects of surfactant properties

Journal of fluid mechanics, 2018-03, Vol.838, p.222-247

2018

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Osteogenesis imperfecta, diagnosis information (clinical and genetic classification)

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2008-06, Vol.15 (5), p.789-791

2008

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Efficacité de l’ouverture du trou occipital chez l’enfant achondroplase : évaluation clinique, radiologique et polysomnographique

Neuro-chirurgie, 2011-09, Vol.57 (4), p.263-263

2011

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Aplasia cutis congenita du scalp : place de la chirurgie précoce dans une série de 40 enfants

Neuro-chirurgie, 2011-09, Vol.57 (4), p.266-266

2011

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Osteocondrodisplasias letales

EMC - Aparato Locomotor, 2016-06, Vol.49 (2), p.1-7

Le Merrer, M.

2016

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Condrodisplasias responsables de insuficiencia estatural

EMC - Aparato Locomotor, 2016-02, Vol.49 (1), p.1-14

Le Merrer, M.

2016

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Osteopatías con alteraciones de la densidad ósea

EMC - Aparato Locomotor, 2016-02, Vol.49 (1), p.1-12

Le Merrer, M.

2016

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Prenatal diagnosis of brachytelephalangic chondrodysplasia punctata: case report

Ultrasound in obstetrics & gynecology, 2009-12, Vol.34 (6), p.724-726

2009

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Atypical findings in Kabuki syndrome: Report of 8 patients in a series of 20 and review of the literature

American journal of medical genetics. Part A, 2004-08, Vol.129A (1), p.64-68

2004

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Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assays

Archives of disease in childhood, 2006-02, Vol.91 (2), p.178-182

2006

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Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families

Journal of medical genetics, 2010-12, Vol.47 (12), p.797-802

2010

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A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34

Human genetics, 2007-04, Vol.121 (2), p.269-273

2007

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Enfant battu ou enfant fragile ?

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2003-08, Vol.10 (8), p.679-680

2003

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In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

Journal of medical genetics, 2003-01, Vol.40 (1), p.34-36

2003

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BBS10 mutations are common in ‘Meckel’-type cystic kidneys

Journal of medical genetics, 2010-12, Vol.47 (12), p.848-852

2010

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Bubbles slipping along a crenelated wall

Viscous mechanism for Leidenfrost propulsion on a ratchet

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

Holes and cracks in rigid foam films

Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patients

Three‐dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasia

Genotype-phenotype correlation in hereditary multiple exostoses

Lamin a Truncation in Hutchinson-Gilford Progeria

Spectrum of NSD1 mutations in Sotos and Weaver syndromes

Slicing softly with shear

Level-set simulations of a 2D topological rearrangement in a bubble assembly: effects of surfactant properties

Osteogenesis imperfecta, diagnosis information (clinical and genetic classification)

Efficacité de l’ouverture du trou occipital chez l’enfant achondroplase : évaluation clinique, radiologique et polysomnographique

Aplasia cutis congenita du scalp : place de la chirurgie précoce dans une série de 40 enfants

Osteocondrodisplasias letales

Condrodisplasias responsables de insuficiencia estatural

Osteopatías con alteraciones de la densidad ósea

Prenatal diagnosis of brachytelephalangic chondrodysplasia punctata: case report

Atypical findings in Kabuki syndrome: Report of 8 patients in a series of 20 and review of the literature

Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assays

Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families

A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34

Enfant battu ou enfant fragile ?

In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

BBS10 mutations are common in ‘Meckel’-type cystic kidneys

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