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	1.	A newly described mutation of the CLCN7 gene causes neuropathic autosomal recessive osteopetrosis in an Arab family. [electronic resource] by Al-Aama, Jumana Y Dabbagh, Amal A Edrees, Alaa Y Producer: 20120601 In: Clinical dysmorphology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia. [electronic resource] by A Gaboon, Nagwa E Bakur, Khadijah H Edrees, Alaa Y Al-Aama, Jumana Y Publication details: Journal of pediatric genetics Sep 2017 In: Journal of pediatric genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Erratum: Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia. [electronic resource] by Gaboon, Nagwa E A Bakur, Khadijah H Edrees, Alaa Y Al-Aama, Jumana Y Publication details: Journal of pediatric genetics Sep 2017 In: Journal of pediatric genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mutations in the pre-replication complex cause Meier-Gorlin syndrome. [electronic resource] by Bicknell, Louise S Bongers, Ernie M H F Leitch, Andrea Brown, Stephen Schoots, Jeroen Harley, Margaret E Aftimos, Salim Al-Aama, Jumana Y Bober, Michael Brown, Paul A J van Bokhoven, Hans Dean, John Edrees, Alaa Y Feingold, Murray Fryer, Alan Hoefsloot, Lies H Kau, Nikolaus Knoers, Nine V A M Mackenzie, James Opitz, John M Sarda, Pierre Ross, Alison Temple, I Karen Toutain, Annick Wise, Carol A Wright, Michael Jackson, Andrew P Producer: 20110509 In: Nature genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis. [electronic resource] by de Munnik, Sonja A Bicknell, Louise S Aftimos, Salim Al-Aama, Jumana Y van Bever, Yolande Bober, Michael B Clayton-Smith, Jill Edrees, Alaa Y Feingold, Murray Fryer, Alan van Hagen, Johanna M Hennekam, Raoul C Jansweijer, Maaike C E Johnson, Diana Kant, Sarina G Opitz, John M Ramadevi, A Radha Reardon, Willie Ross, Alison Sarda, Pierre Schrander-Stumpel, Constance T R M Schoots, Jeroen Temple, I Karen Terhal, Paulien A Toutain, Annick Wise, Carol A Wright, Michael Skidmore, David L Samuels, Mark E Hoefsloot, Lies H Knoers, Nine V A M Brunner, Han G Jackson, Andrew P Bongers, Ernie M H F Producer: 20120921 In: European journal of human genetics : EJHG vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorder. [electronic resource] by de Munnik, Sonja A Otten, Barto J Schoots, Jeroen Bicknell, Louise S Aftimos, Salim Al-Aama, Jumana Y van Bever, Yolande Bober, Michael B Borm, George F Clayton-Smith, Jill Deal, Cheri L Edrees, Alaa Y Feingold, Murray Fryer, Alan van Hagen, Johanna M Hennekam, Raoul C Jansweijer, Maaike C E Johnson, Diana Kant, Sarina G Opitz, John M Ramadevi, A Radha Reardon, Willie Ross, Alison Sarda, Pierre Schrander-Stumpel, Constance T R M Sluiter, A Erik Temple, I Karen Terhal, Paulien A Toutain, Annick Wise, Carol A Wright, Michael Skidmore, David L Samuels, Mark E Hoefsloot, Lies H Knoers, Nine V A M Brunner, Han G Jackson, Andrew P Bongers, Ernie M H F Producer: 20130621 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)