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	401.	ORAL-FACIAL-DIGITAL SYNDROME TYPE I (CLINICAL CASE). [electronic resource] by Horlenko, O Lenchenko, A Kossey, G Tomey, A Debretseni, O Producer: 20190516 In: Georgian medical news no. 285 Availability: No items available. Save to lists Add to cart (remove)
	402.	[The damaging effects of alcoholism on the offspring (author's transl)]. [electronic resource] by Majewski, F Producer: 19781025 In: Der Nervenarzt vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	403.	[Coffin-Lowry syndrome. Description of 2 cases associated with cardiovascular anomalies]. [electronic resource] by Della Cella, G Stagnaro, M G Beluschi, C Forni, G L Producer: 19871029 In: La Pediatria medica e chirurgica : Medical and surgical pediatrics vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	404.	Cranio-carpo-tarsal dysplasia or the whistling face syndrome. II. Oral intercommissural distance in children. [electronic resource] by Cervenka, J Figalová, P Gorlin, R J Producer: 19690426 In: American journal of diseases of children (1960) vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	405.	[Phenotype of trisomy 9]. [electronic resource] by Pfeiffer, R A Müller, R Producer: 19850131 In: Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde vol. 132 Availability: No items available. Save to lists Add to cart (remove)
	406.	Buccal anomalies, cephalometric analysis and genetic study of two sisters with orofaciodigital syndrome type I. [electronic resource] by Romero, Martín Franco, Brunella del Pozo, Jaime Sánchez Romance, Ana Producer: 20080122 In: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	407.	The ciliopathies in neuronal development: a clinical approach to investigation of Joubert syndrome and Joubert syndrome-related disorders. [electronic resource] by Sattar, Shifteh Gleeson, Joseph G Producer: 20110930 In: Developmental medicine and child neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	408.	Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1. [electronic resource] by Lopes, Carla A M Prosser, Suzanna L Romio, Leila Hirst, Robert A O'Callaghan, Chris Woolf, Adrian S Fry, Andrew M Producer: 20110620 In: Journal of cell science vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	409.	An Orofaciodigital Syndrome 1 Patient and Her Mother Carry the Same OFD1 Mutation but Have Different X Chromosome Inactivation Patterns. [electronic resource] by Iijima, Takashi Hayami, Noriko Takaichi, Kenmei Morisada, Naoya Nozu, Kandai Iijima, Kazumoto Sawa, Naoki Hoshino, Junichi Ubara, Yoshifumi Producer: 20200113 In: Internal medicine (Tokyo, Japan) vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	410.	Orodigitofacial syndromes type I and II: clinical and surgical studies. [electronic resource] by Martinot, V L Manouvrier, S Anastassov, Y Ribiere, J Pellerin, P N 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)
	411.	MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone. [electronic resource] by Li, Chunmei Jensen, Victor L Park, Kwangjin Kennedy, Julie Garcia-Gonzalo, Francesc R Romani, Marta De Mori, Roberta Bruel, Ange-Line Gaillard, Dominique Doray, Bérénice Lopez, Estelle Rivière, Jean-Baptiste Faivre, Laurence Thauvin-Robinet, Christel Reiter, Jeremy F Blacque, Oliver E Valente, Enza Maria Leroux, Michel R Producer: 20160810 In: PLoS biology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	412.	X-linked recessive inheritance of an orofaciodigital syndrome with partial expression in females and survival of affected males. [electronic resource] by Edwards, M Mulcahy, D Turner, G Producer: 19890413 In: Clinical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	413.	The ectodermal dysplasias. [electronic resource] by Solomon, L M Cook, B Klipfel, W Producer: 19870427 In: Dermatologic clinics vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	414.	STUDIES OF A FAMILY WITH THE ORAL-FACIAL-DIGITAL SYNDROME. [electronic resource] by DOEGE, T C THULINE, H C PRIEST, J H NORBY, D E BRYANT, J S Producer: 19961201 In: The New England journal of medicine vol. 271 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	415.	Mutations of CEP83 cause infantile nephronophthisis and intellectual disability. [electronic resource] by Failler, Marion Gee, Heon Yung Krug, Pauline Joo, Kwangsic Halbritter, Jan Belkacem, Lilya Filhol, Emilie Porath, Jonathan D Braun, Daniela A Schueler, Markus Frigo, Amandine Alibeu, Olivier Masson, Cécile Brochard, Karine Hurault de Ligny, Bruno Novo, Robert Pietrement, Christine Kayserili, Hulya Salomon, Rémi Gubler, Marie-Claire Otto, Edgar A Antignac, Corinne Kim, Joon Benmerah, Alexandre Hildebrandt, Friedhelm Saunier, Sophie Producer: 20140729 In: American journal of human genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	416.	[Orofaciodigital syndrome. Apropos of an 11th case in the same family]. [electronic resource] by Vissian, L Vaillaud, J C Producer: 19721010 In: Annales de dermatologie et de syphiligraphie vol. 99 Availability: No items available. Save to lists Add to cart (remove)
	417.	[Significance of family photographs for genetic counseling in sex-linked heredity]. [electronic resource] by Le Marec, B Roussey, M Producer: 19841218 In: Journal de genetique humaine vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	418.	Genetics of congenital lip defects. [electronic resource] by Day, D W Producer: 19850109 In: Clinics in plastic surgery vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	419.	Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrum. [electronic resource] by Franceschini, P Guala, A Vardeu, M P Signorile, F Franceschini, D Bolgiani, M P Producer: 19960419 In: American journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	420.	Blepharospasm and limb dystonia caused by Mohr-Tranebjaerg syndrome with a novel splice-site mutation in the deafness/dystonia peptide gene. [electronic resource] by Kim, Hee T Edwards, Mark J Tyson, Jess Quinn, Niall P Bitner-Glindzicz, Maria Bhatia, Kailash P Producer: 20080416 In: Movement disorders : official journal of the Movement Disorder Society vol. 22 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.