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	1.	Regional and ethnic distribution of beta thalassemia mutations and effect of consanguinity in patients referred for prenatal diagnosis. [electronic resource] by Hafeez, Maimoona Aslam, Maleeha Ali, Ayesha Rashid, Yasmin Jafri, Hussain Producer: 20070904 In: Journal of the College of Physicians and Surgeons--Pakistan : JCPSP vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	'All is done by Allah'. Understandings of Down syndrome and prenatal testing in Pakistan. [electronic resource] by Bryant, Louise D Ahmed, Shenaz Ahmed, Mushtaq Jafri, Hussain Raashid, Yasmin Producer: 20110824 In: Social science & medicine (1982) vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Experiences of parents with a child with Down syndrome in Pakistan and their views on termination of pregnancy. [electronic resource] by Ahmed, Shenaz Bryant, Louise D Ahmed, Mushtaq Jafri, Hussain Raashid, Yasmin Producer: 20130108 In: Journal of community genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Pakistani mothers' and fathers' experiences and understandings of the diagnosis of Down syndrome for their child. [electronic resource] by Ahmed, Kiran Jan Ahmed, Mushtaq Jafri, Hussain S Raashid, Yasmin Ahmed, Shenaz Producer: 20150108 In: Journal of community genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36. [electronic resource] by Keen, T Jeffrey Mohamed, Moin D McKibbin, Martin Rashid, Yasmin Jafri, Hussain Maumenee, Irene H Inglehearn, Chris F Producer: 20031224 In: European journal of human genetics : EJHG vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34. [electronic resource] by Hampshire, Daniel J Ayub, Mohammed Springell, Kelly Roberts, Emma Jafri, Hussain Rashid, Yasmin Bond, Jacquelyn Riley, John H Woods, C Geoffrey Producer: 20060623 In: European journal of human genetics : EJHG vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration. [electronic resource] by Ali, Manir Ramprasad, Vedam Lakshmi Soumittra, Nagasamy Mohamed, Moin D Jafri, Hussain Rashid, Yasmin Danciger, Michael McKibbin, Martin Kumaramanickavel, Govindasamy Inglehearn, Chris F Producer: 20090306 In: Molecular vision vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	8.	Genotype-phenotype correlation for leber congenital amaurosis in Northern Pakistan. [electronic resource] by McKibbin, Martin Ali, Manir Mohamed, Moin D Booth, Adam P Bishop, Fiona Pal, Bishwanath Springell, Kelly Raashid, Yasmin Jafri, Hussain Inglehearn, Chris F Producer: 20100127 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mutations in microcephalin cause aberrant regulation of chromosome condensation. [electronic resource] by Trimborn, Marc Bell, Sandra M Felix, Clive Rashid, Yasmin Jafri, Hussain Griffiths, Paul D Neumann, Luitgard M Krebs, Alice Reis, André Sperling, Karl Neitzel, Heidemarie Jackson, Andrew P Producer: 20040920 In: American journal of human genetics vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	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)
	11.	Umbilical vein oxytocin for the treatment of retained placenta (Release Study): a double-blind, randomised controlled trial. [electronic resource] by Weeks, Andrew D Alia, Godfrey Vernon, Gillian Namayanja, Annette Gosakan, Radhika Majeed, Tayyaba Hart, Anna Jafri, Hussain Nardin, Juan Carroli, Guillermo Fairlie, Fiona Raashid, Yasmin Mirembe, Florence Alfirevic, Zarko Producer: 20100304 In: Lancet (London, England) vol. 375 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies. [electronic resource] by Szymanska, Katarzyna Berry, Ian Logan, Clare V Cousins, Simon Rr Lindsay, Helen Jafri, Hussain Raashid, Yasmin Malik-Sharif, Saghira Castle, Bruce Ahmed, Mushtag Bennett, Chris Carlton, Ruth Johnson, Colin A Producer: 20130226 In: Cilia vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Partnerships for better mental health worldwide: WPA recommendations on best practices in working with service users and family carers. [electronic resource] by Wallcraft, Jan Amering, Michaela Freidin, Julian Davar, Bhargavi Froggatt, Diane Jafri, Hussain Javed, Afzal Katontoka, Sylvester Raja, Shoba Rataemane, Solomon Steffen, Sigrid Tyano, Sam Underhill, Christopher Wahlberg, Henrik Warner, Richard Herrman, Helen Producer: 20111103 In: World psychiatry : official journal of the World Psychiatric Association (WPA) vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	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)
	15.	Genetic and epigenetic analysis of recurrent hydatidiform mole. [electronic resource] by Hayward, Bruce E De Vos, Michel Talati, Nargese Abdollahi, M Reza Taylor, Graham R Meyer, Esther Williams, Denise Maher, Eamonn R Setna, Faridon Nazir, Kausar Hussaini, Shahnaz Jafri, Hussain Rashid, Yasmin Sheridan, Eamonn Bonthron, David T Producer: 20090730 In: Human mutation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma. [electronic resource] by Ali, Manir Buentello-Volante, Beatriz McKibbin, Martin Rocha-Medina, J Alberto Fernandez-Fuentes, Narcis Koga-Nakamura, Wilson Ashiq, Aruna Khan, Kamron Booth, Adam P Williams, Grange Raashid, Yasmin Jafri, Hussain Rice, Aine Inglehearn, Chris F Zenteno, Juan Carlos Producer: 20101112 In: Molecular vision vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	17.	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)
	18.	Protein-truncating mutations in ASPM cause variable reduction in brain size. [electronic resource] by Bond, Jacquelyn Scott, Sheila Hampshire, Daniel J Springell, Kelly Corry, Peter Abramowicz, Marc J Mochida, Ganesh H Hennekam, Raoul C M Maher, Eamonn R Fryns, Jean-Pierre Alswaid, Abdulrahman Jafri, Hussain Rashid, Yasmin Mubaidin, Ammar Walsh, Christopher A Roberts, Emma Woods, C Geoffrey Producer: 20040819 In: American journal of human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa. [electronic resource] by Ali, Manir Hocking, Paul M McKibbin, Martin Finnegan, Sorcha Shires, Mike Poulter, James A Prescott, Katrina Booth, Adam Raashid, Yasmin Jafri, Hussain Ruddle, Jonathan B Mackey, David A Jacobson, Samuel G Toomes, Carmel Lester, Douglas H Burt, David W Curry, William J Inglehearn, Chris F Producer: 20111201 In: Investigative ophthalmology & visual science vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	An SCN9A channelopathy causes congenital inability to experience pain. [electronic resource] by Cox, James J Reimann, Frank Nicholas, Adeline K Thornton, Gemma Roberts, Emma Springell, Kelly Karbani, Gulshan Jafri, Hussain Mannan, Jovaria Raashid, Yasmin Al-Gazali, Lihadh Hamamy, Henan Valente, Enza Maria Gorman, Shaun Williams, Richard McHale, Duncan P Wood, John N Gribble, Fiona M Woods, C Geoffrey Producer: 20070111 In: Nature vol. 444 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 28 results.