Your search returned 531 results.

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	301.	Oro-facial-digital syndrome type II. [electronic resource] by Kalyan, Meenakshi Kanitkar, S John, Robby Gireesh, G Bhate, Amit Mithun, M Producer: 20130717 In: The Journal of the Association of Physicians of India vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	302.	Recognition in adult patients of malformations induced by folic-acid antagonists. [electronic resource] by Reich, E W Cox, R P Becker, M H Genieser, N B McCarthy, J G Converse, J M Producer: 19790324 In: Birth defects original article series vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	303.	Rapp-Hodgkin syndrome and AEC syndrome: are they the same entity? [electronic resource] by Cambiaghi, S Tadini, G Barbareschi, M Menni, S Caputo, R Producer: 19940317 In: The British journal of dermatology vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	304.	Autosomal recessive oral-facial-digital syndrome with resemblance to OFD types II, III, IV and VI: a new OFD syndrome? [electronic resource] by Chitayat, D Stalker, H J Azouz, E M Producer: 19930209 In: American journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	305.	Midline malformation syndromes. [electronic resource] by Sharma, A K Phadke, S R Producer: 19940824 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)
	306.	X-linked recessive deafness-dystonia syndrome (Mohr-Tranebjaerg syndrome). [electronic resource] by Tranebjaerg, L Jensen, P K van Ghelue, M Producer: 20001002 In: Advances in oto-rhino-laryngology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	307.	Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephaly. [electronic resource] by Thauvin-Robinet, C Rousseau, T Durand, C Laurent, N Maingueneau, C Faivre, L Sagot, P Nivelon-Chevallier, A Producer: 20010913 In: Prenatal diagnosis vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	308.	The splice c.1815G>A variant in KIAA0586 results in a phenotype bridging short-rib-polydactyly and oral-facial-digital syndrome: A case report and literature review. [electronic resource] by Cocciadiferro, Dario Agolini, Emanuele Digilio, Maria Cristina Sinibaldi, Lorenzo Castori, Marco Silvestri, Evelina Dotta, Andrea Dallapiccola, Bruno Novelli, Antonio Producer: 20200309 In: Medicine vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	309.	Further observations on a pedigree of the oral-facial-digital syndrome. [electronic resource] by Kernohan, D C Dodge, J A Producer: 19700124 In: Archives of disease in childhood vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	310.	Midline defects of the orofaciodigital syndrome type VI (Váradi syndrome). [electronic resource] by Wey, P D Neidich, J A Hoffman, L A LaTrenta, G S Producer: 19950109 In: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	311.	50 Years Ago in The Journal of Pediatrics: The Genetic Basis for the Variability of the Hereditable Diseases. [electronic resource] by Cordeiro, Leonardo Bodurtha, Joann Producer: 20190304 In: The Journal of pediatrics vol. 196 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	312.	[Neurogenic hypernatremia with adipsia and cerebral malformations in a child with ectrodactyly-ectodermal dysplasia-cleft lip-palate syndrome]. [electronic resource] by Ronconi, G F Ronconi, M Stella, M Soffiati, G Pesenti, P Producer: 19860916 In: La Pediatria medica e chirurgica : Medical and surgical pediatrics vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	313.	Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene. [electronic resource] by Ferrante, Maria I Romio, Leila Castro, Silvia Collins, John E Goulding, David A Stemple, Derek L Woolf, Adrian S Wilson, Stephen W Producer: 20090203 In: Human molecular genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	314.	Ablepheron macrostomia syndrome. [electronic resource] by McCarthy, G T West, C M Producer: 19771229 In: Developmental medicine and child neurology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	315.	Orofaciodigital syndrome type I associated with polycystic kidneys and agenesis of the corpus callosum. [electronic resource] by Connacher, A A Forsyth, C C Stewart, W K Producer: 19870520 In: Journal of medical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	316.	A female infant with features of Mohr and Majewski syndromes: variable expression, a genetic compound, or a distinct entity? [electronic resource] by Baraitser, M Burn, J Fixsen, J Producer: 19830623 In: Journal of medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	317.	Seckel syndrome in a Yemeni family in Saudi Arabia. [electronic resource] by Krishna, A G Scrimgeour, E M Zawawi, T H Producer: 19940923 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	318.	The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3. [electronic resource] by Feather, S A Woolf, A S Donnai, D Malcolm, S Winter, R M Producer: 19970828 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	319.	Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative study. [electronic resource] by Thauvin-Robinet, C Cossée, M Cormier-Daire, V Van Maldergem, L Toutain, A Alembik, Y Bieth, E Layet, V Parent, P David, A Goldenberg, A Mortier, G Héron, D Sagot, P Bouvier, A M Huet, F Cusin, V Donzel, A Devys, D Teyssier, J R Faivre, L Producer: 20061215 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	320.	Oral-facial-digital syndrome, with polycystic kidneys and liver: pathological and cytogenetic studies. [electronic resource] by Tucker, C C Finley, S C Tucker, E S Finley, W H Producer: 19670526 In: Journal of medical genetics vol. 3 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 531 results.