Your search returned 531 results.

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	341.	Temporal bone findings in a case of otopalatodigital syndrome. [electronic resource] by Shi, S R Producer: 19850401 In: Archives of otolaryngology (Chicago, Ill. : 1960) vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	342.	Multiple recurrent and de novo odontogenic keratocysts associated with oral-facial-digital syndrome. [electronic resource] by Lindeboom, Jerome A H Kroon, Frans H M de Vires, Jan van den Akker, Hans P Producer: 20030717 In: Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	343.	[Brachmann-de Lange syndrome: report of 4 cases in Mexican children]. [electronic resource] by Villegas-Camargo, I Lacro, R V Lyons-Jones, K Producer: 19880311 In: Boletin medico del Hospital Infantil de Mexico vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	344.	[Stickler's syndrome]. [electronic resource] by Balagi, C Nieri, S Prestandrea, C Tomà, P Rossi, P Oldani, R Cottafava, F Producer: 19880624 In: Minerva pediatrica vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	345.	[Oro-digito-facial syndrome. Apropos of a case]. [electronic resource] by Corfu, G Millard, C Producer: 19731005 In: Annales d'oto-laryngologie et de chirurgie cervico faciale : bulletin de la Societe d'oto-laryngologie des hopitaux de Paris vol. 90 Availability: No items available. Save to lists Add to cart (remove)
	346.	Jeune syndrome with tongue lobulation and preaxial polydactyly, and Jeune syndrome with situs inversus and asplenia: compound heterozygosity Jeune-Mohr and Jeune-Ivemark? [electronic resource] by Majewski, E Oztürk, B Gillessen-Kaesbach, G Producer: 19960925 In: American journal of medical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	347.	Deoxyribonucleic acid contamination in archival human temporal bones: a potentially significant problem. [electronic resource] by McKenna, Michael J Kristiansen, Arthur G Tropitzsch, Anke S Tranebjaerg, Lisbeth Merchant, Saumil N Producer: 20021129 In: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	348.	Oral-facial-digital syndrome type 1, Caroli's disease and cystic renal disease. [electronic resource] by Toprak, Omer Uzum, Atilla Cirit, Mustafa Esi, Ertap Inci, Ayca Ersoy, Rifki Tanrisev, Mehmet Ok, Ercan Franco, Brunella Producer: 20061122 In: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	349.	Otolaryngologic findings in whistling face syndrome. [electronic resource] by Marasovich, W A Mazaheri, M Stool, S E Producer: 19891130 In: Archives of otolaryngology--head & neck surgery vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	350.	Orofaciodigital syndrome type IV: report of a patient. [electronic resource] by Nevin, N C Thomas, P S Producer: 19890427 In: American journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	351.	Mohr syndrome in two siblings. [electronic resource] by Gencík, A Gencíkova, A Producer: 19840227 In: Journal de genetique humaine vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	352.	[Case of Arskog is syndrome]. [electronic resource] by Chen, T P Romanenko, O P Shats, V Ia Sandomirskaia, L M Azarova, V Ia Producer: 19800815 In: Pediatriia no. 4 Availability: No items available. Save to lists Add to cart (remove)
	353.	Complete congenital bony syngnathia in a case of oromandibular limb hypogenesis syndrome. [electronic resource] by Knoll, B Karas, D Persing, J A Shin, J Producer: 20010531 In: The Journal of craniofacial surgery vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	354.	Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia. A new syndrome? [electronic resource] by Castro, Carlos H B C Freitas, Patrícia Z Antoneli, Melissa Z Santiago, Giselda Ribeiro, Lucilene A Richieri-Costa, Antonio Producer: 20051221 In: Clinical dysmorphology vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	355.	Orofaciodigital syndrome type IV (Mohr-Majewski syndrome): report of a family with two affected siblings. [electronic resource] by Kahl, Philip Heukamp, Lukas Carl Buettner, Reinhard Friedrichs, Nicolaus Roesing, Bettina Knopfle, Gisela Producer: 20070725 In: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	356.	Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes. [electronic resource] by Bruel, Ange-Line Franco, Brunella Duffourd, Yannis Thevenon, Julien Jego, Laurence Lopez, Estelle Deleuze, Jean-François Doummar, Diane Giles, Rachel H Johnson, Colin A Huynen, Martijn A Chevrier, Véronique Burglen, Lydie Morleo, Manuela Desguerres, Isabelle Pierquin, Geneviève Doray, Bérénice Gilbert-Dussardier, Brigitte Reversade, Bruno Steichen-Gersdorf, Elisabeth Baumann, Clarisse Panigrahi, Inusha Fargeot-Espaliat, Anne Dieux, Anne David, Albert Goldenberg, Alice Bongers, Ernie Gaillard, Dominique Argente, Jesús Aral, Bernard Gigot, Nadège St-Onge, Judith Birnbaum, Daniel Phadke, Shubha R Cormier-Daire, Valérie Eguether, Thibaut Pazour, Gregory J Herranz-Pérez, Vicente Goldstein, Jaclyn S Pasquier, Laurent Loget, Philippe Saunier, Sophie Mégarbané, André Rosnet, Olivier Leroux, Michel R Wallingford, John B Blacque, Oliver E Nachury, Maxence V Attie-Bitach, Tania Rivière, Jean-Baptiste Faivre, Laurence Thauvin-Robinet, Christel Producer: 20180307 In: Journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	357.	Novel double-deletion mutations of the OFD1 gene creating multiple novel transcripts. [electronic resource] by Morisawa, Takeshi Yagi, Mariko Surono, Agus Yokoyama, Naoki Ohmori, Makoto Terashi, Hiroto Matsuo, Masafumi Producer: 20040908 In: Human genetics vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	358.	[Hypoglossia-hypodactylia. Apropos of a case associated with Moebius' syndrome and temporomandibular ankylosis]. [electronic resource] by Campistol, J Molina, V Gonzalez, A Rissech, M Baraibar, R Krauel, J Producer: 19800923 In: Pediatrie vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	359.	Full-field electroretinograms in a family with Mohr-Tranebjaerg syndrome. [electronic resource] by Ponjavic, V Andreasson, S Tranebjaerg, L Lubs, H A Producer: 19970331 In: Acta ophthalmologica Scandinavica vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	360.	Oral-facial-digital (OFD) syndrome with associated features: a new syndrome or genetic heterogeneity and variability? [electronic resource] by Morán-Barroso, V Valdés Flores, M García-Cavazos, R Kofman-Alfaro, S Saavedra-Ontiveros, D Producer: 19980413 In: Clinical dysmorphology vol. 7 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 531 results.