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	1161.	Pre- and postnatal growth retardation, scaling skin, moderate mental retardation and quadrispasticity, hypospadias grade 2 and hydro-uretero nephrosis, postaxial polydactyly. A distinct MCA/MR syndrome? [electronic resource] by Fryns, J P Lagae, L Rizzo, W B Producer: 19990208 In: Clinical dysmorphology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1162.	Choroideremia with polydactyly mimicking the Laurence-Moon-Bardet-Biedl syndrome. [electronic resource] by Schwartz, Stephen G Noble, Kenneth G Carr, Ronald E Producer: 20031006 In: Retina (Philadelphia, Pa.) vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1163.	Meckel-Gruber syndrome: pathologic manifestations, minimal diagnostic criteria, and differential diagnosis. [electronic resource] by Alexiev, Borislav A Lin, Xiaoqing Sun, Chen-Chih Brenner, David S Producer: 20060831 In: Archives of pathology & laboratory medicine vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1164.	Laurin-Sandrow syndrome: review and redefinition. [electronic resource] by Mariño-Enríquez, Adrián Lapunzina, Pablo Omeñaca, Félix Morales, Carmen Rodríguez, José I Producer: 20081113 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1165.	Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum. [electronic resource] by Cavalcanti, Denise P Huber, Celine Sang, Kim-Hanh Le Quan Baujat, Geneviève Collins, Felicity Delezoide, Anne-Lise Dagoneau, Nathalie Le Merrer, Martine Martinovic, Jelena Mello, Marcos Fernando S Vekemans, Michel Munnich, Arnold Cormier-Daire, Valerie Producer: 20110602 In: Journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1166.	Outcome of two types of surgical correction of the extra phalanx in triphalangeal thumb: is there a difference? [electronic resource] by Zuidam, J M Selles, R W de Kraker, M Hovius, S E R Producer: 20161219 In: The Journal of hand surgery, European volume vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1167.	Current Scope of Practice for Newborn Care in Non-Intensive Hospital Settings. [electronic resource] by Chung, Esther K Gable, E Kaye Golden, W Christopher Hudson, Jennifer A Hackman, Nicole M Andrews, Jennifer P Jackson, DeeAnne S Beavers, Jessica B Mirchandani, Dipti R Kellams, Ann Krevitsky, Meredith E Monroe, Kimberly Madlon-Kay, Diane J Stratbucker, William Campbell, Deborah Collins, Jolene Rauch, Daniel Producer: 20170926 In: Hospital pediatrics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1168.	Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype. [electronic resource] by Ponzi, Emanuela Asaro, Alessia Orteschi, Daniela Genuardi, Maurizio Zollino, Marcella Gurrieri, Fiorella Producer: 20160429 In: European journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1169.	A gene for Meckel syndrome maps to chromosome 11q13. [electronic resource] by Roume, J Genin, E Cormier-Daire, V Ma, H W Mehaye, B Attie, T Razavi-Encha, F Fallet-Bianco, C Buenerd, A Clerget-Darpoux, F Munnich, A Le Merrer, M Producer: 19981204 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1170.	Trisomy 2p syndrome: a fetus with anencephaly and postaxial polydactyly. [electronic resource] by Hahm, G K Barth, R F Schauer, G M Reiss, R Opitz, J M Producer: 19991201 In: American journal of medical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1171.	Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly. [electronic resource] by Lettice, Laura A Horikoshi, Taizo Heaney, Simon J H van Baren, Marijke J van der Linde, Herma C Breedveld, Guido J Joosse, Marijke Akarsu, Nurten Oostra, Ben A Endo, Naoto Shibata, Minoru Suzuki, Mikio Takahashi, Eiichi Shinka, Toshikatsu Nakahori, Yutaka Ayusawa, Dai Nakabayashi, Kazuhiko Scherer, Stephen W Heutink, Peter Hill, Robert E Noji, Sumihare Producer: 20020701 In: Proceedings of the National Academy of Sciences of the United States of America vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1172.	[Hall syndrome (Pallister-Hall syndrome)]. [electronic resource] by Kuniba, Hideo Egashira, Masanori Motomura, Hideki Motomura, Katsuaki Kondoh, Tatsuro Producer: 20070109 In: Nihon rinsho. Japanese journal of clinical medicine vol. Suppl 3 Availability: No items available. Save to lists Add to cart (remove)
	1173.	Thumb duplication - simple surgery for a common problem? [electronic resource] by Benatar, N Producer: 20040908 In: Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1174.	[Genetic analysis of a Chinese pedigree with congenital synpolydactyly]. [electronic resource] by Qin, Wei Shu, An-Li Xing, Qing-He Yang, Mao-Sheng Feng, Guo-Yin He, Lin Producer: 20040211 In: Yi chuan xue bao = Acta genetica Sinica vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	1175.	Type A ulnar polydactyly of the hand: a classification system and clinical series. [electronic resource] by Pritsch, Tamir Ezaki, Marybeth Mills, Janith Oishi, Scott N Producer: 20130823 In: The Journal of hand surgery vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1176.	IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome. [electronic resource] by Zhang, Wenjuan Taylor, S Paige Nevarez, Lisette Lachman, Ralph S Nickerson, Deborah A Bamshad, Michael Krakow, Deborah Cohn, Daniel H Producer: 20170720 In: Human molecular genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1177.	Long-Term Clinical and Radiographic Follow-Up of Preaxial Polydactyly Reconstruction. [electronic resource] by Gholson, J Joseph Shah, Apurva S Buckwalter, Joseph A Buckwalter, Joseph A Producer: 20200218 In: The Journal of hand surgery vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1178.	Robot-assisted repair of a urogenital sinus with an anorectal malformation in a patient with McKusick-Kaufman syndrome. [electronic resource] by Phillips, Michael R Linden, Allison F Vinocur, Charles D Hagerty, Jennifer A Producer: 20200924 In: Journal of pediatric urology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1179.	De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bones. [electronic resource] by Delatycki, M B Danks, A Churchyard, A Zhou, X-P Eng, C Producer: 20031103 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1180.	Postaxial polydactyly, ulnar ray dysgenesis, and renal cystic dysplasia in sibs. [electronic resource] by Kaplan, B S Bellah, R D Producer: 20000309 In: American journal of medical genetics vol. 87 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1610 results.