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	1201.	Extending the phenotypic spectrum of CHARGE syndrome: a case with preaxial polydactyly. [electronic resource] by Douglas, Andrew G L Lam, Wayne Producer: 20100222 In: Clinical dysmorphology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1202.	Mutations in DYNC2H1, the cytoplasmic dynein 2, heavy chain 1 motor protein gene, cause short-rib polydactyly type I, Saldino-Noonan type. [electronic resource] by Badiner, N Taylor, S P Forlenza, K Lachman, R S Bamshad, M Nickerson, D Cohn, D H Krakow, D Producer: 20180418 In: Clinical genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1203.	GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families. [electronic resource] by Patel, Rashmi Singh, Chandra Bhan Bhattacharya, Visweswar Singh, Subodh Kumar Ali, Akhtar Producer: 20161213 In: Congenital anomalies vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1204.	Does timing of surgery influence the long-term results of foot polydactyly treatment? [electronic resource] by Kubat, Ozren Antičević, Darko Producer: 20190624 In: Foot and ankle surgery : official journal of the European Society of Foot and Ankle Surgeons vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1205.	A GLI3 variant leading to polydactyly in heterozygotes and Pallister-Hall-like syndrome in a homozygote. [electronic resource] by Kariminejad, Ariana Ghaderi-Sohi, Siavash Keshavarz, Elham Hashemi, Seyed Abolghasem Parsimehr, Elham Szenker-Ravi, Emmanuelle Khatoo, Muznah Faraji Zonooz, Mehrshid Reversade, Bruno Najmabadi, Hossein Hennekam, Raoul C Producer: 20210604 In: Clinical genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1206.	Neuro-glial neurotrophic interaction in the S-100 beta retarded mutant mouse (Polydactyly Nagoya). III. Transplantation study. [electronic resource] by Ueda, S Aikawa, M Kawata, M Naruse, I Whitaker-Azmitia, P M Azmitia, E C Producer: 19970325 In: Brain research vol. 738 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1207.	A TCTN2 mutation defines a novel Meckel Gruber syndrome locus. [electronic resource] by Shaheen, Ranad Faqeih, Eissa Seidahmed, Mohammed Z Sunker, Asma Alali, Faten Ezzat AlQahtani, Khadijah Alkuraya, Fowzan S Producer: 20110919 In: Human mutation vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1208.	Central polydactyly of the foot: surgical management with plantar and dorsal advancement flaps. [electronic resource] by Osborn, Emily J Davids, Jon R Leffler, Lauren C Gibson, Thomas W Pugh, Linda I Producer: 20150512 In: Journal of pediatric orthopedics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1209.	McKusik-Kaufman syndrome: prenatal diagnosis, genetics and follow up. [electronic resource] by Gaucherand, Pascal Vavasseur-Monot, Chantal Ollagnon, Elizabeth Boisson, Catherine Labaune, Jean-Marc Basset, Thierry Yared, George Producer: 20030429 In: Prenatal diagnosis vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1210.	Isolated polydactyly: prenatal diagnosis and perinatal outcome. [electronic resource] by Bromley, B Shipp, T D Benacerraf, B Producer: 20010104 In: Prenatal diagnosis vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1211.	Teratogenic effects of static magnetic field on mouse fetuses. [electronic resource] by Saito, Kenichi Suzuki, Hiroetsu Suzuki, Katsushi Producer: 20060925 In: Reproductive toxicology (Elmsford, N.Y.) vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1212.	Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype? [electronic resource] by Makrythanasis, Periklis Gimelli, Stefania Béna, Frédérique Dahoun, Sophie Morris, Michael A Antonarakis, Stylianos E Bottani, Armand Producer: 20120605 In: European journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1213.	A novel gene (FAM20B encoding glycosaminoglycan xylosylkinase) for neonatal short limb dysplasia resembling Desbuquois dysplasia. [electronic resource] by Kuroda, Yukiko Murakami, Hiroaki Enomoto, Yumi Tsurusaki, Yoshinori Takahashi, Kazumi Mitsuzuka, Kanako Ishimoto, Hitoshi Nishimura, Gen Kurosawa, Kenji Producer: 20200805 In: Clinical genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1214.	Recurrent short rib-polydactyly syndrome with unusual associations. [electronic resource] by Shindel, B Wise, S Producer: 19990413 In: Journal of clinical ultrasound : JCU vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1215.	Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis. [electronic resource] by Kuss, Pia Villavicencio-Lorini, Pablo Witte, Florian Klose, Joachim Albrecht, Andrea N Seemann, Petra Hecht, Jochen Mundlos, Stefan Producer: 20090310 In: The Journal of clinical investigation vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1216.	Hydrolethalus syndrome, in contrast to Smith-Lemli-Opitz syndrome, is not due to a defect in post-squalene cholesterol biosynthesis: a case report. [electronic resource] by Rakheja, Dinesh Cimo, Michael L Ramus, Ronald M Rogers, Beverly B Bennett, Michael J Boyer, Philip J Galindo, Rene L Producer: 20050318 In: American journal of medical genetics. Part A vol. 129A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1217.	A trisomy 13 case with Robertsonian translocation presenting with atypical findings. [electronic resource] by Demirel, G Oguz, S S Celik, I H Sandal, G Uras, N Erdeve, O Dilmen, U Producer: 20101123 In: Genetic counseling (Geneva, Switzerland) vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	1218.	Molecular Genetics of Sex Identification, Breed Ancestry and Polydactyly in the Norwegian Lundehund Breed. [electronic resource] by Kropatsch, Regina Melis, Claudia Stronen, Astrid V Jensen, Henrik Epplen, Joerg T Producer: 20150928 In: The Journal of heredity vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1219.	Polydactyly: phenotypes, genetics and classification. [electronic resource] by Malik, S Producer: 20151026 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1220.	Common Pediatric Congenital Conditions of the Hand. [electronic resource] by Kozin, Scott H Zlotolow, Dan A Producer: 20151020 In: Plastic and reconstructive surgery vol. 136 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 1610 results.