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	21.	Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects. [electronic resource] by Newton, R Stanier, P Loughna, S Henderson, D J Forbes, S A Farrall, M Jensson, O Moore, G E Producer: 19941004 In: Clinical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	SOME SUGGESTIONS FOR NATIONAL SERVICE ON THE PART OF ZOOLOGISTS AND ZOOLOGICAL LABORATORIES. [electronic resource] by Conklin, E G Forbes, S A Kofoid, C A Lillie, F R Morgan, T H Parker, G H Reighard, J Smith, H M Producer: 20100702 In: Science (New York, N.Y.) vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	The Catalogue of Somatic Mutations in Cancer (COSMIC). [electronic resource] by Forbes, S A Bhamra, G Bamford, S Dawson, E Kok, C Clements, J Menzies, A Teague, J W Futreal, P A Stratton, M R Producer: 20080523 In: Current protocols in human genetics vol. Chapter 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3. [electronic resource] by Forbes, S A Brennan, L Richardson, M Coffey, A Cole, C G Gregory, S G Bentley, D R Mumm, S Moore, G E Stanier, P Producer: 19961024 In: Genomics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. [electronic resource] by Pannett, A A J Kennedy, A M Turner, J J O Forbes, S A Cavaco, B M Bassett, J H D Cianferotti, L Harding, B Shine, B Flinter, F Maidment, C G H Trembath, R Thakker, R V Producer: 20030613 In: Clinical endocrinology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Characterization of mutations in patients with multiple endocrine neoplasia type 1. [electronic resource] by Bassett, J H Forbes, S A Pannett, A A Lloyd, S E Christie, P T Wooding, C Harding, B Besser, G M Edwards, C R Monson, J P Sampson, J Wass, J A Wheeler, M H Thakker, R V Producer: 19980406 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1). [electronic resource] by Courseaux, A Grosgeorge, J Gaudray, P Pannett, A A Forbes, S A Williamson, C Bassett, D Thakker, R V Teh, B T Farnebo, F Shepherd, J Skogseid, B Larsson, C Giraud, S Zhang, C X Salandre, J Calender, A Producer: 19970327 In: Genomics vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	28.	Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1). [electronic resource] by Forbes, S A Pannett, A A Bassett, J H Harding, B Wooding, C Thakker, R V Butler, R Ogilvie, D Anand, R Gaudray, P Weber, G Larsson, C Zhang, C X Calender, A Höppener, J W Lips, C J Kas, K Producer: 19970925 In: Human genetics vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	COSMIC: High-Resolution Cancer Genetics Using the Catalogue of Somatic Mutations in Cancer. [electronic resource] by Forbes, S A Beare, D Bindal, N Bamford, S Ward, S Cole, C G Jia, M Kok, C Boutselakis, H De, T Sondka, Z Ponting, L Stefancsik, R Harsha, B Tate, J Dawson, E Thompson, S Jubb, H Campbell, P J Producer: 20180312 In: Current protocols in human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1. [electronic resource] by Höppener, J W De Wit, M J Simarro-Doorten, A Y Roijers, J F van Herrewaarden, H M Lips, C J Parente, F Quincey, D Gaudray, P Khodaei, S Weber, G Teh, B Farnebo, F Larsson, C Zhang, C X Calender, A Pannett, A A Forbes, S A Bassett, J H Thakker, R V Lemmens, I Van de Ven, W J Kas, K Producer: 19981001 In: Genomics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)