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	81.	Genotype-phenotype correlation in hereditary multiple exostoses. [electronic resource] by Francannet, C Cohen-Tanugi, A Le Merrer, M Munnich, A Bonaventure, J Legeai-Mallet, L Producer: 20011205 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Three new cases of the Schinzel-Giedion syndrome and review of the literature. [electronic resource] by Labrune, P Lyonnet, S Zupan, V Imbert, M C Goutieres, F Hubert, P Le Merrer, M Producer: 19940519 In: American journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	COL9A3: A third locus for multiple epiphyseal dysplasia. [electronic resource] by Paassilta, P Lohiniva, J Annunen, S Bonaventure, J Le Merrer, M Pai, L Ala-Kokko, L Producer: 20000405 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Progressive osseous heteroplasia. Report of a family. [electronic resource] by Urtizberea, J A Testart, H Cartault, F Boccon-Gibod, L Le Merrer, M Kaplan, F S Producer: 19981020 In: The Journal of bone and joint surgery. British volume vol. 80 Availability: No items available. Save to lists Add to cart (remove)
	85.	Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy. [electronic resource] by Castelnau, P Le Merrer, M Diatloff-Zito, C Marquis, E Tête, M J Robert, J J Producer: 20001222 In: European journal of pediatrics vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	Genitopatellar syndrome: a new condition comprising absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardation. [electronic resource] by Cormier-Daire, V Chauvet, M L Lyonnet, S Briard, M L Munnich, A Le Merrer, M Producer: 20000828 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasia. [electronic resource] by Heinz-Erian, P Schmidt, H Le Merrer, M Phillips, A D Kiess, W Hadorn, H B Producer: 19990331 In: Journal of pediatric gastroenterology and nutrition vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	CFC syndrome: a syndrome distinct from Noonan syndrome. [electronic resource] by Verloes, A Le Merrer, M Soyeur, D Kaplan, J Pangalos, C Rigo, J Briard, M L Producer: 19890309 In: Annales de genetique vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	89.	[Association of VACTERL and hydrocephalus: a new familial entity]. [electronic resource] by Briard, M L le Merrer, M Plauchu, H Dodinval, P Lambotte, C Moraine, C Serville, F Producer: 19850320 In: Annales de genetique vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	90.	Genetic mapping of Xp22.12-p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL). [electronic resource] by Heuertz, S Smahi, A Wilkie, A O Le Merrer, M Maroteaux, P Hors-Cayla, M C Producer: 19951120 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia. [electronic resource] by Jobert, A S Zhang, P Couvineau, A Bonaventure, J Roume, J Le Merrer, M Silve, C Producer: 19980723 In: The Journal of clinical investigation vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	Presentation of six cases of Stüve-Wiedemann syndrome. [electronic resource] by Cormier-Daire, V Munnich, A Lyonnet, S Rustin, P Delezoide, A L Maroteaux, P Le Merrer, M Producer: 19990105 In: Pediatric radiology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study. [electronic resource] by Verloes, A Aymé, S Gambarelli, D Gonzales, M Le Merrer, M Mulliez, N Philip, N Roume, J Producer: 19910906 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	[Exclusion prenatal diagnosis of chronic familial septic granulomatosis]. [electronic resource] by Pham Huu, T Dumez, Y Durand, A Le Merrer, M Lemerle-Gruson, S Hakim, J Griscelli, C Producer: 19850628 In: Archives francaises de pediatrie vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	95.	Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome. [electronic resource] by El Ghouzzi, V Lajeunie, E Le Merrer, M Cormier-Daire, V Renier, D Munnich, A Bonaventure, J Producer: 19990513 In: European journal of human genetics : EJHG vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	The orocraniodigital syndrome of Juberg and Hayward. [electronic resource] by Verloes, A Le Merrer, M Davin, J C Wittamer, P Abrassart, C Bricteux, G Briard, M L Producer: 19920618 In: Journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	97.	Genetic heterogeneity of Meckel syndrome. [electronic resource] by Roume, J Ma, H W Le Merrer, M Cormier-Daire, V Girlich, D Genin, E Munnich, A Producer: 19980204 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	98.	IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies. [electronic resource] by Vilain, E Le Merrer, M Lecointre, C Desangles, F Kay, M A Maroteaux, P McCabe, E R Producer: 20000107 In: The Journal of clinical endocrinology and metabolism vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Clinical and genetic heterogeneity of hypochondroplasia. [electronic resource] by Rousseau, F Bonaventure, J Legeai-Mallet, L Schmidt, H Weissenbach, J Maroteaux, P Munnich, A Le Merrer, M Producer: 19970204 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome. [electronic resource] by Cormier-Daire, V Le Merrer, M Gigarel, N Morichon, N Prieur, M Lyonnet, S Vekemans, M Munnich, A Producer: 19970508 In: American journal of medical genetics vol. 69 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.