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	1521.	Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway. [electronic resource] by Patterson, Victoria L Damrau, Christine Paudyal, Anju Reeve, Benjamin Grimes, Daniel T Stewart, Michelle E Williams, Debbie J Siggers, Pam Greenfield, Andy Murdoch, Jennifer N Producer: 20090714 In: Human molecular genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1522.	A novel H395R mutation in MKKS/BBS6 causes retinitis pigmentosa and polydactyly without other findings of Bardet-Biedl or McKusick-Kaufman syndrome. [electronic resource] by Hulleman, John D Nguyen, Annie Ramprasad, V L Murugan, Sakthivel Gupta, Ravi Mahindrakar, Avinash Angara, Ravi Sankurathri, Chandrasekhar Mootha, V Vinod Producer: 20161013 In: Molecular vision vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	1523.	Heterozygous pathogenic variants in GLI1 are a common finding in isolated postaxial polydactyly A/B. [electronic resource] by Palencia-Campos, Adrián Martínez-Fernández, María-Luisa Altunoglu, Umut Soto-Bielicka, Patricia Torres, Antonio Marín, Purificación Aller, Elena Şentürk, Leyli Berköz, Ömer Yıldıran, Mehmet Kayserili, Hülya Gil-Camarero, Elena Colli-Lista, Gloria Sanchís-Calvo, Amparo Carretero, Alba Guillén-Navarro, Encarna López-González, Vanesa Ballesta-Martínez, María Rosell, Jordi Aglan, Mona S Temtamy, Samia Otaify, Ghada A Cuevas-Catalina, Lourdes Torres-Saavedra, María-Nieves Nevado, Julian Tenorio, Jair Lapunzina, Pablo Bermejo-Sánchez, Eva Ruiz-Pérez, Víctor L Producer: 20210519 In: Human mutation vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1524.	The chicken talpid3 gene encodes a novel protein essential for Hedgehog signaling. [electronic resource] by Davey, Megan G Paton, I Robert Yin, Yili Schmidt, Maike Bangs, Fiona K Morrice, David R Smith, Terence Gordon Buxton, Paul Stamataki, Despina Tanaka, Mikiko Münsterberg, Andrea E Briscoe, James Tickle, Cheryll Burt, Dave W Producer: 20060705 In: Genes & development vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1525.	Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: report of a novel mutation of the PCNT gene. [electronic resource] by Piane, Maria Della Monica, Matteo Piatelli, Gianluca Lulli, Patrizia Lonardo, Fortunato Chessa, Luciana Scarano, Gioacchino Producer: 20100106 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1526.	Clinical findings in patients with GLI2 mutations--phenotypic variability. [electronic resource] by Bertolacini, C D P Ribeiro-Bicudo, L A Petrin, A Richieri-Costa, A Murray, J C Producer: 20120405 In: Clinical genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1527.	Expression and regulation of eHAND during limb development. [electronic resource] by Fernandez-Teran, Marian Piedra, M Elisa Rodriguez-Rey, Jose C Talamillo, Ana Ros, Maria A Producer: 20031229 In: Developmental dynamics : an official publication of the American Association of Anatomists vol. 226 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1528.	Gonadal mosaicism in severe Pallister-Hall syndrome. [electronic resource] by Ng, David Johnston, Jennifer J Turner, Joyce T Boudreau, Eilis A Wiggs, Edythe A Theodore, William H Biesecker, Leslie G Producer: 20040728 In: American journal of medical genetics. Part A vol. 124A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1529.	Prenatal Diagnosis of Hydro(metro)colpos: A Series of 20 Cases. [electronic resource] by Mallmann, Michael R Reutter, Heiko Mack-Detlefsen, Birte Gottschalk, Ingo Geipel, Annegret Berg, Christoph Boemers, Thomas M Gembruch, Ulrich Producer: 20190422 In: Fetal diagnosis and therapy vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1530.	Preaxial polydactyly following early gestational exposure to the smoothened agonist, SAG, in C57BL/6J mice. [electronic resource] by Fish, Eric W Parnell, Scott E Sulik, Kathleen K Baker, Lorinda K Murdaugh, Laura B Lamson, David Williams, Kevin P Producer: 20180312 In: Birth defects research vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1531.	Mutation analysis and description of sixteen RSH/Smith-Lemli-Opitz syndrome patients: polymerase chain reaction-based assays to simplify genotyping. [electronic resource] by Krakowiak, P A Nwokoro, N A Wassif, C A Battaile, K P Nowaczyk, M J Connor, W E Maslen, C Steiner, R D Porter, F D Producer: 20001026 In: American journal of medical genetics vol. 94 Availability: No items available. Save to lists Add to cart (remove)
	1532.	Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly. [electronic resource] by Qu, S Tucker, S C Ehrlich, J S Levorse, J M Flaherty, L A Wisdom, R Vogt, T F Producer: 19980827 In: Development (Cambridge, England) vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1533.	Direct interaction with Hoxd proteins reverses Gli3-repressor function to promote digit formation downstream of Shh. [electronic resource] by Chen, Yuting Knezevic, Vladimir Ervin, Valerie Hutson, Richard Ward, Yvona Mackem, Susan Producer: 20040818 In: Development (Cambridge, England) vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1534.	A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region. [electronic resource] by Yang, Yi-Feng Ai, Qi Huang, Can Chen, Jin-Lan Wang, Jian Xie, Li Zhang, Wei-Zhi Yang, Jin-Fu Tan, Zhi-Ping Producer: 20131113 In: Gene vol. 528 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1535.	Translational repression of the McKusick-Kaufman syndrome transcript by unique upstream open reading frames encoding mitochondrial proteins with alternative polyadenylation sites. [electronic resource] by Akimoto, Chizuru Sakashita, Eiji Kasashima, Katsumi Kuroiwa, Kenji Tominaga, Kaoru Hamamoto, Toshiro Endo, Hitoshi Producer: 20130620 In: Biochimica et biophysica acta vol. 1830 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1536.	The disruption of a novel limb cis-regulatory element of SHH is associated with autosomal dominant preaxial polydactyly-hypertrichosis. [electronic resource] by Petit, Florence Jourdain, Anne-Sophie Holder-Espinasse, Muriel Keren, Boris Andrieux, Joris Duterque-Coquillaud, Martine Porchet, Nicole Manouvrier-Hanu, Sylvie Escande, Fabienne Producer: 20160919 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1537.	Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations. [electronic resource] by Tapper, William J Foulds, Nicola Cross, Nicholas C P Aranaz, Paula Score, Joannah Hidalgo-Curtis, Claire Robinson, David O Gibson, Jane Ennis, Sarah Temple, I Karen Collins, Andrew Producer: 20141028 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1538.	Polydactyly. [electronic resource] by Rac, Martha W F McKinney, Jennifer Gandhi, Manisha Producer: 20200318 In: American journal of obstetrics and gynecology vol. 221 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1539.	Strike three for GLI3. [electronic resource] by Biesecker, L G Producer: 19971204 In: Nature genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1540.	Suppressor of Fused Is Required for Determining Digit Number and Identity via Gli3/Fgfs/Gremlin. [electronic resource] by Li, Jianying Wang, Qihui Cui, Ying Yang, Xueqin Li, Yan Zhang, Xiaoyun Qiu, Mengsheng Zhang, Ze Zhang, Zunyi Producer: 20160421 In: PloS one vol. 10 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.