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	1.	An autosomal recessive syndrome of severe cognitive impairment, dysmorphic facies and skeletal abnormalities maps to the long arm of chromosome 17. [electronic resource] by Al-Owain, M Alazami, A M Alkuraya, F S Producer: 20120615 In: Clinical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Excessively redundant umbilical skin as a potential early clinical feature of Morquio syndrome and FKBP14-related Ehlers-Danlos syndrome. [electronic resource] by Aldeeri, A A Alazami, A M Hijazi, H Alzahrani, F Alkuraya, F S Producer: 20150618 In: Clinical genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel syndromic form of sensory-motor polyneuropathy is linked to chromosome 22q13.31-q13.33. [electronic resource] by Bohlega, S Alazami, A M Cupler, E Al-Hindi, H Ibrahim, E Alkuraya, F S Producer: 20110308 In: Clinical genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	NPHP4 mutation is linked to cerebello-oculo-renal syndrome and male infertility. [electronic resource] by Alazami, A M Alshammari, M J Baig, M Salih, M A Hassan, H H Alkuraya, F S Producer: 20150512 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome. [electronic resource] by Steindl, K Alazami, A M Bhatia, K P Wuerfel, J T Petersen, D Cartolari, R Neri, G Klein, C Mongiardo, B Alkuraya, F S Schneider, S A Producer: 20110222 In: Clinical genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients. [electronic resource] by Alazami, A M Schneider, S A Bonneau, D Pasquier, L Carecchio, M Kojovic, M Steindl, K de Kerdanet, M Nezarati, M M Bhatia, K P Degos, B Goh, E Alkuraya, F S Producer: 20110222 In: Clinical genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield. [electronic resource] by Anazi, S Maddirevula, S Faqeih, E Alsedairy, H Alzahrani, F Shamseldin, H E Patel, N Hashem, M Ibrahim, N Abdulwahab, F Ewida, N Alsaif, H S Al Sharif, H Alamoudi, W Kentab, A Bashiri, F A Alnaser, M AlWadei, A H Alfadhel, M Eyaid, W Hashem, A Al Asmari, A Saleh, M M AlSaman, A Alhasan, K A Alsughayir, M Al Shammari, M Mahmoud, A Al-Hassnan, Z N Al-Husain, M Osama Khalil, R Abd El Meguid, N Masri, A Ali, R Ben-Omran, T El Fishway, P Hashish, A Ercan Sencicek, A State, M Alazami, A M Salih, M A Altassan, N Arold, S T Abouelhoda, M Wakil, S M Monies, D Shaheen, R Alkuraya, F S Producer: 20171010 In: Molecular psychiatry vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)