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	1.	Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome. [electronic resource] by El-Ruby, M Hemly, N A Zaki, M S Producer: 20071016 In: Genetic counseling (Geneva, Switzerland) vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	2.	Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes. [electronic resource] by Zaki, M S Kamel, A A El-Ruby, M Producer: 20060404 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	3.	Bartsocas-Papas syndrome with variable expressivity in an Egyptian family. [electronic resource] by Zaki, M S Kamel, A K Effat, L K El-Ruby, M O Producer: 20120828 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical and cytogenetic study of a non mosaic 46, X, isodicentric Yq in an Egyptian patient with Turner syndrome. [electronic resource] by El-Bassyouni, H T El-Gerzawy, A Eid, O El-Ruby, M O Producer: 20130627 In: Genetic counseling (Geneva, Switzerland) vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	5.	Klinefelter syndrome, rare variant 49, XXXXY. [electronic resource] by Salman, H Abanamy, A Khan, N Basset, G Choudhury, A H El-Ruby, M O Producer: 20121002 In: Annals of Saudi medicine vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION. [electronic resource] by Eid, M O Eid, M M Kamel, A K El-Ruby, M Abdel-Salam, G M H Producer: 20151001 In: Genetic counseling (Geneva, Switzerland) vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	7.	Screening of genital anomalies in newborns and infants in two egyptian governorates. [electronic resource] by Mazen, I El-Ruby, M Kamal, R El-Nekhely, I El-Ghandour, M Tantawy, S El-Gammal, M Producer: 20100730 In: Hormone research in paediatrics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Emanuel syndrome due to unusual segregation of paternal origin. [electronic resource] by Zaki, M S Mohamed, A M Kamel, A K El-Gerzawy, A M S El-Ruby, M O Producer: 20120828 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	9.	Detection and putative effect of GATA4 gene variants in patients with congenital cardiac septal defects. [electronic resource] by Al-Azzouny, M A El Ruby, M O Issa, H A Behiry, E G Elsayed, N R Fayez, A G Producer: 20170201 In: Cellular and molecular biology (Noisy-le-Grand, France) vol. 62 Availability: No items available. Save to lists Add to cart (remove)
	10.	Growth charts of Egyptian children with Down syndrome (0-36 months). [electronic resource] by Meguid, N A El-Kotoury, A I S Abdel-Salam, G M H El-Ruby, M O Afifi, H H Producer: 20051108 In: Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	11.	Ring chromosome 15: expanding the phenotype. [electronic resource] by Eid, M M El-Bassyouni, H T Eid, O M Hamad, S A Elgerzawy, A Zaki, M S El-Ruby, M Producer: 20140312 In: Genetic counseling (Geneva, Switzerland) vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	12.	Phenotypic and cytogenetic spectrum of 9p trisomy. [electronic resource] by Temtamy, S A Kamel, A K Ismail, S Helmy, N A Aglan, M S El Gammal, M El Ruby, M Mohamed, A M Producer: 20070621 In: Genetic counseling (Geneva, Switzerland) vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	13.	Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study. [electronic resource] by El-Bassyouni, H T El-Gerzawy, A M S Mohamed, A M Kamel, A K Hussein, H A Thomas, M M El-Ruby, M Producer: 20140812 In: Genetic counseling (Geneva, Switzerland) vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	14.	Spectrum of mutations in the ANTXR2 (CMG2) gene in infantile systemic hyalinosis and juvenile hyaline fibromatosis. [electronic resource] by El-Kamah, G Y Fong, K El-Ruby, M Afifi, H H Clements, S E Lai-Cheong, J E Amr, K El-Darouti, M McGrath, J A Producer: 20101222 In: The British journal of dermatology vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Unique karyotype: mos 46,X,dic(X;Y)(p22.33;p11.32)/ 45,X/45,dic(X;Y)(p22.33;p11.32) in an Egyptian patient with Ovotesticular disorder of sexual development. [electronic resource] by Mazen, I M Kamel, A K Mohamed, A M Hussien, H A Essawi, M L Hassan, H A El-Ruby, M O Aref, A Mekkawy, M K Producer: 20140131 In: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	The most encountered groups of genetic disorders in Giza Governorate, Egypt. [electronic resource] by Afifi, H H El-Ruby, M O El-Bassyouni, H T Ismail, S I Aglan, M S El-Harouni, A A Mazen, I M Zaki, M S Bassiouni, R I Hosny, L A El-Kamah, G Y El-Kotoury, A I Ashour, A M Abdel-Salam, G M El-Gammal, M A Hamed, K Kamal, R M El-Nekhely, I Temtamy, S A Producer: 20100518 In: Bratislavske lekarske listy vol. 111 Availability: No items available. Save to lists Add to cart (remove)