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	41.	Incomplete penetrance and expressivity skewing in hereditary multiple exostoses. [electronic resource] by Legeai-Mallet, L Munnich, A Maroteaux, P Le Merrer, M Producer: 19971002 In: Clinical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Metaphyseal acroscyphodysplasia. [electronic resource] by Verloes, A Le Merrer, M Farriaux, J P Maroteaux, P Producer: 19910904 In: Clinical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Lethal progeroid syndrome with osteolysis. Case report. [electronic resource] by Le Merrer, M Guillot, M Briard, M L Maroteaux, P Producer: 19920113 In: Annales de genetique vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	44.	Recessive metaphyseal dysplasia without hypotrichosis. A syndrome clinically distinct from McKusick cartilage-hair hypoplasia. [electronic resource] by Verloes, A Pierard, G E Le Merrer, M Maroteaux, P Producer: 19910305 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Digito-reno-cerebral syndrome: confirmation of Eronen syndrome. [electronic resource] by Le Merrer, M David, A Goutieres, F Briard, M L Producer: 19921201 In: Clinical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	[Epidemiological and genetic study of 3 congenital cardiopathies with neonatal disclosure]. [electronic resource] by Briard, M L Chauvet, M L Le Merrer, M Frezal, J Producer: 19840907 In: Archives francaises de pediatrie vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	47.	[Osteogenesis imperfecta, diagnosis information (clinical and genetic classification)]. [electronic resource] by Baujat, G Lebre, A-S Cormier-Daire, V Le Merrer, M Producer: 20080916 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	[Autosomal recessive metaphyseal chondrodysplasia and Hirschsprung's disease]. [electronic resource] by le Merrer, M Briard, M L Chauvet, M L Maroteaux, P Producer: 19910425 In: Annales de pediatrie vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	49.	[Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia]. [electronic resource] by Rousseau, F Bonaventure, J Le Merrer, M Maroteaux, P Munnich, A Producer: 19970130 In: Annales d'endocrinologie vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	50.	[Trigonocephaly: isolated, associated and syndromic forms. Genetic study in a series of 278 patients]. [electronic resource] by Lajeunie, E Le Merrer, M Arnaud, E Marchac, D Renier, D Producer: 19981124 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Neural tube defects in France: segregation analysis. [electronic resource] by Demenais, F Le Merrer, M Briard, M L Elston, R C Producer: 19820708 In: American journal of medical genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	[Genetic counseling in craniostenosis. Results of a prospective study performed with a group of studies on craniofacial malformations]. [electronic resource] by Le Merrer, M Ledinot, V Renier, D Marchac, D Briard, M L Producer: 19890321 In: Journal de genetique humaine vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	53.	[Pregnancy abnormalities as alerting signs of Steinert's congenital myotonic dystrophy]. [electronic resource] by Briard, M L Le Merrer, M Goutieres, F Aicardi, J Frézal, J Producer: 19810421 In: Journal de genetique humaine vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	54.	Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcome. [electronic resource] by Renier, D El-Ghouzzi, V Bonaventure, J Le Merrer, M Lajeunie, E Producer: 20000425 In: Journal of neurosurgery vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	Acral dysostosis dyserythropoiesis syndrome. [electronic resource] by Le Merrer, M Girot, R Parent, P Cormier-Daire, V Maroteaux, P Producer: 19950921 In: European journal of pediatrics vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	56.	[Malformation uropathies and multiple malformation syndromes]. [electronic resource] by Briard, M L Le Merrer, M Kaplan, J Bois, E Frézal, J Producer: 19840817 In: Journal de genetique humaine vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	57.	[Epidemiologic and genetic studies of spina bifida (author's transl)]. [electronic resource] by Le Merrer, M Briard, M L Demenais, F Feingold, J Frézal, J Producer: 19810224 In: Archives francaises de pediatrie vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	58.	Genetic study of scaphocephaly. [electronic resource] by Lajeunie, E Le Merrer, M Bonaïti-Pellie, C Marchac, D Renier, D Producer: 19961213 In: American journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Genetic study of nonsyndromic coronal craniosynostosis. [electronic resource] by Lajeunie, E Le Merrer, M Bonaïti-Pellie, C Marchac, D Renier, D Producer: 19950626 In: American journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	Long-term follow-up in a patient with metatropic dysplasia. [electronic resource] by Geneviève, D Le Merrer, M Munnich, A Maroteaux, P Cormier-Daire, V Producer: 20050705 In: American journal of medical genetics. Part A vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 187 results.