Your search returned 21 results.

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	1.	Meta-analyses of the association of HLA-DRB1 alleles with rheumatoid arthritis among Arabs. [electronic resource] by Bizzari, Sami Nair, Pratibha Al Ali, Mahmoud Taleb Hamzeh, Abdul Rezzak Producer: 20180501 In: International journal of rheumatic diseases vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Expanded PCH1D phenotype linked to EXOSC9 mutation. [electronic resource] by Bizzari, Sami Hamzeh, Abdul Rezzak Mohamed, Madiha Al-Ali, Mahmoud Taleb Bastaki, Fatma Producer: 20200930 In: European journal of medical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	CTGA: the database for genetic disorders in Arab populations. [electronic resource] by Tadmouri, Ghazi O Al Ali, Mahmoud Taleb Al-Haj Ali, Sarah Al Khaja, Najib Producer: 20060228 In: Nucleic acids research vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Marinesco-Sjögren Syndrome in an Emirati Child with a Novel Mutation in SIL1 Affecting the 5' Untranslated Region. [electronic resource] by Nair, Pratibha Hamzeh, Abdul Rezzak Mohamed, Madiha Tawfiq, Nafisa Al-Ali, Mahmoud Taleb Bastaki, Fatma Producer: 20170920 In: Medical principles and practice : international journal of the Kuwait University, Health Science Centre vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference. [electronic resource] by Nair, Pratibha Bizzari, Sami Rajah, Nirmal Assaf, Nada Al-Ali, Mahmoud Taleb Hamzeh, Abdul Rezzak Producer: 20161107 In: Journal of translational medicine vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Erratum to: Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis. [electronic resource] by Nair, Pratibha Hamzeh, Abdul Rezzak Mohamed, Madiha Malik, Ethar Mustafa Al-Ali, Mahmoud Taleb Bastaki, Fatma Publication details: Metabolic brain disease Oct 2016 In: Metabolic brain disease vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis. [electronic resource] by Nair, Pratibha Hamzeh, Abdul Rezzak Mohamed, Madiha Malik, Ethar Mustafa Al-Ali, Mahmoud Taleb Bastaki, Fatma Producer: 20180108 In: Metabolic brain disease vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa. [electronic resource] by Nair, Pratibha Hamzeh, Abdul Rezzak Malik, Ethar Mustafa Oberoi, Darshjit Al-Ali, Mahmoud Taleb Bastaki, Fatma Publication details: Oman journal of ophthalmology In: Oman journal of ophthalmology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Identification of a novel homozygous UNC80 variant in a child with infantile hypotonia with psychomotor retardation and characteristic facies-2 (IHPRF2). [electronic resource] by Obeid, Tasneem Hamzeh, Abdul Rezzak Saif, Fatima Nair, Pratibha Mohamed, Madiha Al-Ali, Mahmoud Taleb Bastaki, Fatma Producer: 20190205 In: Metabolic brain disease vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A novel nonsense GPSM2 mutation in a Yemeni family underlying Chudley-McCullough syndrome. [electronic resource] by Hamzeh, Abdul Rezzak Nair, Pratibha Mohamed, Madiha Saif, Fatima Tawfiq, Nafisa Al-Ali, Mahmoud Taleb Bastaki, Fatma Producer: 20170210 In: European journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Identification of a novel CTCF mutation responsible for syndromic intellectual disability - a case report. [electronic resource] by Bastaki, Fatma Nair, Pratibha Mohamed, Madiha Malik, Ethar Mustafa Helmi, Mustafa Al-Ali, Mahmoud Taleb Hamzeh, Abdul Rezzak Producer: 20170724 In: BMC medical genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A novel, putatively null, FGD1 variant leading to Aarskog-Scott syndrome in a family from UAE. [electronic resource] by Hamzeh, Abdul Rezzak Saif, Fatima Nair, Pratibha Binjab, Asma Jassim Mohamed, Madiha Al-Ali, Mahmoud Taleb Bastaki, Fatma Producer: 20171227 In: BMC pediatrics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis-lymphedema-telangiectasia syndrome by Whole Exome Sequencing. [electronic resource] by Bastaki, Fatma Mohamed, Madiha Nair, Pratibha Saif, Fatima Tawfiq, Nafisa Al-Ali, Mahmoud Taleb Brandau, Oliver Hamzeh, Abdul Rezzak Producer: 20161101 In: Molecular and cellular probes vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A Novel Variant in the Endothelin-Converting Enzyme-Like 1 (ECEL1) Gene in an Emirati Child. [electronic resource] by Hamzeh, Abdul Rezzak Nair, Pratibha Mohamed, Madiha Saif, Fatima Tawfiq, Nafisa Khalifa, Mohamed Al-Ali, Mahmoud Taleb Bastaki, Fatma Producer: 20171011 In: Medical principles and practice : international journal of the Kuwait University, Health Science Centre vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Microcephalic primordial dwarfism in an Emirati patient with PNKP mutation. [electronic resource] by Nair, Pratibha Hamzeh, Abdul Rezzak Mohamed, Madiha Saif, Fatima Tawfiq, Nafisa El Halik, Majdi Al-Ali, Mahmoud Taleb Bastaki, Fatma Producer: 20171024 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates. [electronic resource] by Bastaki, Fatma Nair, Pratibha Mohamed, Madiha Khadora, Manal Mustafa Saif, Fatima Tawfiq, Nafisa Al-Ali, Mahmoud Taleb Hamzeh, Abdul Rezzak Producer: 20170428 In: Hormone research in paediatrics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22). [electronic resource] by Mégarbané, André Hmaimess, Ghassan Bizzari, Sami El-Bazzal, Lara Al-Ali, Mahmoud Taleb Stora, Samantha Delague, Valerie El-Hayek, Stephany Producer: 20200206 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Genomics into Healthcare: the 5th Pan Arab Human Genetics Conference and 2013 Golden Helix Symposium. [electronic resource] by Fortina, Paolo Al Khaja, Najib Al Ali, Mahmoud Taleb Hamzeh, Abdul Rezzak Nair, Pratibha Innocenti, Federico Patrinos, George P Kricka, Larry J Producer: 20141212 In: Human mutation vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Single-center experience of N-linked Congenital Disorders of Glycosylation with a Summary of Molecularly Characterized Cases in Arabs. [electronic resource] by Bastaki, Fatma Bizzari, Sami Hamici, Sana Nair, Pratibha Mohamed, Madiha Saif, Fatima Malik, Ethar Mustafa Al-Ali, Mahmoud Taleb Hamzeh, Abdul Rezzak Producer: 20180101 In: Annals of human genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Further Delineation of the [electronic resource] by Nair, Pratibha El-Bazzal, Lara Mansour, Hicham Sabbagh, Sandra Al-Ali, Mahmoud Taleb Gambarini, Alicia Delague, Valerie El-Hayek, Stephany Mégarbané, André Publication details: Journal of pediatric genetics Dec 2019 In: Journal of pediatric genetics vol. 8 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 21 results.