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	1.	So you want to be ... an oral medicine physician. [electronic resource] by Hegarty, Anne M Mighell, Alan J Producer: 20100421 In: British journal of hospital medicine (London, England : 2005) vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Phenotypic changes associated with DYNACTIN-2 (DCTN2) over expression characterise SJSA-1 osteosarcoma cells. [electronic resource] by Bransfield, Kieran L Askham, Jon M Leek, Jack P Robinson, Philip A Mighell, Alan J Producer: 20060606 In: Molecular carcinogenesis vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. [electronic resource] by Poulter, James A El-Sayed, Walid Shore, Roger C Kirkham, Jennifer Inglehearn, Chris F Mighell, Alan J Producer: 20150212 In: European journal of human genetics : EJHG vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Expression of mOb1, a novel atypical 73 amino acid K50-homeodomain protein, during mouse development. [electronic resource] by Adu, Jimi Leong, Fong T Smith, Neil R Leek, Jack P Markham, Alexander F Robinson, Philip A Mighell, Alan J Producer: 20160423 In: Mechanisms of development vol. 119 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Expression of mOb1, a novel atypical 73 amino acid K50-homeodomain protein, during mouse development. [electronic resource] by Adu, Jimi Leong, Fong T Smith, Neil R Leek, Jack P Markham, Alexander F Robinson, Philip A Mighell, Alan J Producer: 20030414 In: Gene expression patterns : GEP vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta. [electronic resource] by Poulter, James A Brookes, Steven J Shore, Roger C Smith, Claire E L Abi Farraj, Layal Kirkham, Jennifer Inglehearn, Chris F Mighell, Alan J Producer: 20141118 In: Human molecular genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta. [electronic resource] by Poulter, James A Murillo, Gina Brookes, Steven J Smith, Claire E L Parry, David A Silva, Sandra Kirkham, Jennifer Inglehearn, Chris F Mighell, Alan J Producer: 20150603 In: Human molecular genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations. [electronic resource] by de la Dure-Molla, Muriel Quentric, Mickael Yamaguti, Paulo Marcio Acevedo, Ana-Carolina Mighell, Alan J Vikkula, Miikka Huckert, Mathilde Berdal, Ariane Bloch-Zupan, Agnes Producer: 20141112 In: Orphanet journal of rare diseases vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta. [electronic resource] by El-Sayed, Walid Parry, David A Shore, Roger C Ahmed, Mushtaq Jafri, Hussain Rashid, Yasmin Al-Bahlani, Suhaila Al Harasi, Sharifa Kirkham, Jennifer Inglehearn, Chris F Mighell, Alan J Producer: 20091222 In: American journal of human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta. [electronic resource] by Parry, David A Poulter, James A Logan, Clare V Brookes, Steven J Jafri, Hussain Ferguson, Christopher H Anwari, Babra M Rashid, Yasmin Zhao, Haiqing Johnson, Colin A Inglehearn, Chris F Mighell, Alan J Producer: 20130404 In: American journal of human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Real-time PCR based on SYBR-Green I fluorescence: an alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions. [electronic resource] by Ponchel, Frederique Toomes, Carmel Bransfield, Kieran Leong, Fong T Douglas, Susan H Field, Sarah L Bell, Sandra M Combaret, Valerie Puisieux, Alain Mighell, Alan J Robinson, Philip A Inglehearn, Chris F Isaacs, John D Markham, Alex F Producer: 20040621 In: BMC biotechnology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Identification of microcephalin, a protein implicated in determining the size of the human brain. [electronic resource] by Jackson, Andrew P Eastwood, Helen Bell, Sandra M Adu, Jimi Toomes, Carmel Carr, Ian M Roberts, Emma Hampshire, Daniel J Crow, Yanick J Mighell, Alan J Karbani, Gulshan Jafri, Hussain Rashid, Yasmin Mueller, Robert F Markham, Alexander F Woods, C Geoffrey Producer: 20020726 In: American journal of human genetics vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta. [electronic resource] by Parry, David A Mighell, Alan J El-Sayed, Walid Shore, Roger C Jalili, Ismail K Dollfus, Hélène Bloch-Zupan, Agnes Carlos, Roman Carr, Ian M Downey, Louise M Blain, Katharine M Mansfield, David C Shahrabi, Mehdi Heidari, Mansour Aref, Parissa Abbasi, Mohsen Michaelides, Michel Moore, Anthony T Kirkham, Jennifer Inglehearn, Chris F Producer: 20090323 In: American journal of human genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta. [electronic resource] by Parry, David A Brookes, Steven J Logan, Clare V Poulter, James A El-Sayed, Walid Al-Bahlani, Suhaila Al Harasi, Sharifa Sayed, Jihad Raïf, El Mostafa Shore, Roger C Dashash, Mayssoon Barron, Martin Morgan, Joanne E Carr, Ian M Taylor, Graham R Johnson, Colin A Aldred, Michael J Dixon, Michael J Wright, J Tim Kirkham, Jennifer Inglehearn, Chris F Mighell, Alan J Producer: 20121217 In: American journal of human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)