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Trends in Genetics : TIG|September 28, 1999
Genetics of limb anomalies in humansS Manouvrier-Hanu, M Holder-Espinasse, S LyonnetClinical Genetics|February 3, 2006
Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genesP Verdyck, B Blaumeiser, M Holder-Espinasse, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 3, 2012
[Pseudohypoaldosteronisme type I: a rare cause of failure to thrive]A-F Derache, S Rousseau, M Holder-Espinasse, et al.European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|June 9, 2004
Familial syndromic duodenal atresia: Feingold syndromeM Holder-Espinasse, Z Ahmad, J Hamill, et al.The Journal of Pediatrics|October 13, 2001
Pierre Robin sequence: a series of 117 consecutive casesM Holder-Espinasse, V Abadie, V Cormier-Daire, et al.Clinical Dysmorphology|October 23, 2001
Absent lacrimal ducts, distichiasis, dysmorphic features, and brachydactyly: a case reportM Holder-Espinasse, M C de Blois, L Faivre, et al.Clinical Genetics|January 6, 2011
Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndromeF Petit, M Holder-Espinasse, B Duban-Bedu, et al.Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur|April 13, 2006
[Genetics and orthopedics: genetic implications of congenital limb abnormalities]M Holder-Espinasse, B Herbaux, A Mezel, et al.European Journal of Medical Genetics|October 8, 2009
Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imagingM J Alao, D Bonneau, M Holder-Espinasse, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|September 14, 2010
[Prenatal diagnosis of hyperechogenic kidneys: A study of 17 cases]V Emmanuelli, A Lahoche-Manucci, M Holder-Espinasse, et al.Pageof 2