Your search returned 10 results.

Results
	1.	Partial trisomy of the distal part of 10q: a report of two Egyptian cases. [electronic resource] by Aglan, M S Kamel, A K Helmy, N A Producer: 20080909 In: Genetic counseling (Geneva, Switzerland) vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	2.	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)
	3.	Molecular hydrogen production from amorphous solid water during low energy electron irradiation. [electronic resource] by Gadallah, Kamel A K Marchione, Demian Koehler, Sven P K McCoustra, Martin R S Producer: 20180131 In: Physical chemistry chemical physics : PCCP vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	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)
	5.	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)
	6.	Bladder exstrophy and extreme genital anomaly in a patient with pure terminal 1q deletion: expansion of phenotypic spectrum. [electronic resource] by Zaki, M S Gillessen-Kaesbach, G Vater, I Caliebe, A Siebert, R Kamel, A K Mohamed, A M Mazen, I Producer: 20120605 In: European journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	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)
	8.	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)
	9.	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)
	10.	Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation. [electronic resource] by Mohamed, A M El-Bassyouni, H T El-Gerzawy, A M Hammad, S A Helmy, N A Kamel, A K Ismail, S I Issa, M Y Eid, O Zaki, M S Publication details: Molecular cytogenetics 2018 In: Molecular cytogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)