Your search returned 1610 results.

Results
	1541.	Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families. [electronic resource] by Beales, P L Warner, A M Hitman, G A Thakker, R Flinter, F A Producer: 19970505 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1542.	Teratogenicity and developmental toxicity of chlorpyrifos. Maternal exposure during organogenesis in mice. [electronic resource] by Tian, Ying Ishikawa, Hitoshi Yamaguchi, Tomoko Yamauchi, Toru Yokoyama, Kazuhito Producer: 20050816 In: Reproductive toxicology (Elmsford, N.Y.) vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1543.	Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60. [electronic resource] by McInerney-Leo, Aideen M Schmidts, Miriam Cortés, Claudio R Leo, Paul J Gener, Blanca Courtney, Andrew D Gardiner, Brooke Harris, Jessica A Lu, Yeping Marshall, Mhairi Scambler, Peter J Beales, Philip L Brown, Matthew A Zankl, Andreas Mitchison, Hannah M Duncan, Emma L Wicking, Carol Producer: 20131105 In: American journal of human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1544.	Gata6-Dependent GLI3 Repressor Function is Essential in Anterior Limb Progenitor Cells for Proper Limb Development. [electronic resource] by Hayashi, Shinichi Akiyama, Ryutaro Wong, Julia Tahara, Naoyuki Kawakami, Hiroko Kawakami, Yasuhiko Producer: 20170317 In: PLoS genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1545.	Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19. [electronic resource] by Bredrup, Cecilie Saunier, Sophie Oud, Machteld M Fiskerstrand, Torunn Hoischen, Alexander Brackman, Damien Leh, Sabine M Midtbø, Marit Filhol, Emilie Bole-Feysot, Christine Nitschké, Patrick Gilissen, Christian Haugen, Olav H Sanders, Jan-Stephan F Stolte-Dijkstra, Irene Mans, Dorus A Steenbergen, Eric J Hamel, Ben C J Matignon, Marie Pfundt, Rolph Jeanpierre, Cécile Boman, Helge Rødahl, Eyvind Veltman, Joris A Knappskog, Per M Knoers, Nine V A M Roepman, Ronald Arts, Heleen H Producer: 20120221 In: American journal of human genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1546.	The influence of the genetic background on the interaction of retinoic acid with Lx mutation of the rat. [electronic resource] by Bíla, V Kren, V Liska, F Producer: 20010329 In: Folia biologica vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	1547.	Overlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis. [electronic resource] by Killoran, C E Abbott, M McKusick, V A Biesecker, L G Producer: 20010301 In: Clinical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1548.	A female with complete lack of Müllerian fusion, postaxial polydactyly, and tetralogy of fallot: genetic heterogeneity of McKusick-Kaufman syndrome or a unique syndrome? [electronic resource] by Slavotinek, Anne M Dutra, Amalia Kpodzo, Dzifa Pak, Evgenia Nakane, Takaya Turner, Joyce Whiteford, Margo Biesecker, Leslie G Stratton, Pamela Producer: 20050105 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)
	1549.	High-resolution identification of balanced and complex chromosomal rearrangements by 4C technology. [electronic resource] by Simonis, Marieke Klous, Petra Homminga, Irene Galjaard, Robert-Jan Rijkers, Erik-Jan Grosveld, Frank Meijerink, Jules P P de Laat, Wouter Producer: 20091203 In: Nature methods vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1550.	Bardet-Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations. [electronic resource] by Morisada, Naoya Hamada, Riku Miura, Kenichiro Ye, Ming Juan Nozu, Kandai Hattori, Motoshi Iijima, Kazumoto Producer: 20210831 In: CEN case reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1551.	Skeletal development is regulated by fibroblast growth factor receptor 1 signalling dynamics. [electronic resource] by Hajihosseini, Mohammad K Lalioti, Maria D Arthaud, Sandrine Burgar, Helen R Brown, Jill M Twigg, Stephen R F Wilkie, Andrew O M Heath, John K Producer: 20040310 In: Development (Cambridge, England) vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1552.	Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactyly. [electronic resource] by Lodder, Elisabeth M Eussen, Bert H van Hassel, Daniëlla A C M Hoogeboom, A Jeannette M Poddighe, Pino J Coert, J Henk Oostra, Ben A de Klein, Annelies de Graaff, Esther Producer: 20091224 In: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1553.	Preaxial polydactyly of the upper limb viewed as a spectrum of severity of embryonic events. [electronic resource] by Al-Qattan, Mohammad M Producer: 20140227 In: Annals of plastic surgery vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1554.	Overgrowth Syndromes Caused by Somatic Variants in the Phosphatidylinositol 3-Kinase/AKT/Mammalian Target of Rapamycin Pathway. [electronic resource] by Akgumus, Gozde Chang, Fengqi Li, Marilyn M Producer: 20180327 In: The Journal of molecular diagnostics : JMD vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1555.	Alteration of programmed cell death and gene expression by 5-bromodeoxyuridine during limb development in mice. [electronic resource] by Nakamura, N Fujioka, M Mori, C Producer: 20001005 In: Toxicology and applied pharmacology vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1556.	Misexpression of dHAND induces ectopic digits in the developing limb bud in the absence of direct DNA binding. [electronic resource] by McFadden, David G McAnally, John Richardson, James A Charité, Jeroen Olson, Eric N Producer: 20020812 In: Development (Cambridge, England) vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1557.	Holoprosencephaly-Polydactyly syndrome: in search of an etiology. [electronic resource] by Cordero, Dwight R Bendavid, Claude Shanske, Alan L Haddad, Bassem R Muenke, Maximilian Producer: 20080624 In: European journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1558.	Direct functional consequences of ZRS enhancer mutation combine with secondary long range SHH signalling effects to cause preaxial polydactyly. [electronic resource] by Johnson, Edward J Neely, David M Dunn, Ian C Davey, Megan G Producer: 20140919 In: Developmental biology vol. 392 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1559.	BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge. [electronic resource] by Moore, Carrie B Wallace, John R Frase, Alex T Pendergrass, Sarah A Ritchie, Marylyn D Producer: 20131018 In: BMC medical genomics vol. 6 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1560.	Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins. [electronic resource] by Brémond-Gignac, Dominique Gérard-Blanluet, Marion Copin, Henri Bitoun, Pierre Baumann, Clarisse Crolla, J A Benzacken, Brigitte Verloes, Alain Producer: 20050627 In: American journal of medical genetics. Part A vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
69
70
71
72
73
74
75
76
77
78
79
80
81
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1610 results.