Changing Pattern of Fascioliasis Prevalence Early in the 3Rd Millennium in Dakahlia Governorate , Egypt: An Update von Adarosy , H. A, El-Baz , S. A, Gad , Y. Z, El-Shazly , A. M

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A novel point mutation of the androgen receptor (F804L) in an Egyptian newborn with complete androgen insensitivity associated with congenital glaucoma and hypertrophic pyloric ste... von Gad, YZ, Mazen, I, Lumbroso, S, Temtamy, SA, Sultan, C

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A Novel Nonsense Mutation in Exon 1 of HSD17B3 Gene in an Egyptian 46,XY Adult Female Presenting with Primary Amenorrhea von Hassan, H.A., Mazen, I., Gad, Y.Z., Ali, O.S.M., Mekkawy, M., Essawi, M.L.

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Detection of the G34R Mutation in the 5 Alpha Reductase 2 Gene by Allele Specific PCR and Its Linkage to the 89L Allele among Egyptian Cases von Gad, Y.Z., Khairt, R., Mazen, I., Osman, H.G.

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Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria von Effat, L K, Essawi, M L, Abd El Hamid, M S, Hawari, N, Gad, Y Z

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Revisiting the harem conspiracy and death of Ramesses III: anthropological, forensic, radiological, and genetic study von Hawass, Zahi, Ismail, Somaia, Selim, Ashraf, Saleem, Sahar N, Fathalla, Dina, Wasef, Sally, Gad, Ahmed Z, Saad, Rama, Fares, Suzan, Amer, Hany, Gostner, Paul, Gad, Yehia Z, Pusch, Carsten M, Zink, Albert R

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Molecular analysis of androgen resistance syndromes in Egyptian patients von ESSAWI, M, GAD, Y. Z, EL-ROUBY, O, TEMTAMY, S. A, SABOUR, Y. A, EL-AWADY, M. K

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Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells von EL-AWADY, Mostafa K, GAD, Yehia Z, YANPING WEN, EASSAWI, Mona, EFFAT, Laila, AMR, Khalda S, ISMAIL, Somaia, CHRIST, George J

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5α‐Reductase deficiency in patients with micropenis von Gad, Y. Z., Nasr, H., Mazen, I., Salah, N., El‐Ridi, R.

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Studies of up-regulation of androgen receptors in genital skin fibroblasts von Gad, Yehia Z., Berkovitz, Gary D., Migeon, Claude J., Brown, Terry R.

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5 alpha-reductase deficiency in patients with micropenis von Gad, Y Z, Nasr, H, Mazen, I, Salah, N, el-Ridi, R

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Familial Leydig Cell Hypoplasia as a Cause of Male Pseudohermaphroditism von El-Awady, Mostafa K., Temtamy, Samia A., Salam, Moushira A., Gad, Yehia Z.

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Molecular analysis of 5α-reductase type 2 gene in eight unrelated egyptian children with suspected 5α-reductase deficiency: prevalence of the G34R mutation von Mazen, Inas, Gad, Yehia Z., Hafez, Mona, Sultan, Charles, Lumbroso, Serge

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A Novel Double Mutation in the Luteinizing Hormone Receptor in a Kindred with Familial Leydig Cell Hypoplasia and Male Pseudohermaphroditism von Pals-Rylaarsdam, Robin, Liu, Guoquan, Brickman, Wendy, Duranteau, Lise, Monroe, Jason, El-Awady, Mostafa K., Gad, Yehia Z., Shenker, Andrew

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Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1 von Abdel‐Aziz, Nahla, El‐Kamah, Ghada, Khairat, Rabab, Mohamed, Hanan, Gad, Yehia, El‐Ghor, Akmal M., Amr, Khalda S.

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Insights from ancient DNA analysis of Egyptian human mummies: clues to disease and kinship von Gad, Yehia Z, Hassan, Naglaa Abu-Mandil, Mousa, Dalia M, Fouad, Fayrouz A, El-Sayed, Safaa G, Abdelazeem, Marwa A, Mahdy, Samah M, Othman, Hend Y, Ibrahim, Dina W, Khairat, Rabab, Ismail, Somaia

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An intronic DHCR7 genetic polymorphism associates with vitamin D serum level and incidence of acute coronary syndrome von Elbehairy, Mariam M., Abdelnasser, Hala Y., Hanafi, Rasha S., Hassanein, Sally I., Gad, Mohamed Z.

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Karonudib is a promising anticancer therapy in hepatocellular carcinoma von Hua, Xiangwei, Sanjiv, Kumar, Gad, Helge, Pham, Therese, Gokturk, Camilla, Rasti, Azita, Zhao, Zhenjun, He, Kang, Feng, Mingxuan, Zang, Yunjin, Zhang, Jianjun, Xia, Qiang, Helleday, Thomas, Warpman Berglund, Ulrika

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Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt von El-Kamah, Ghada Y, Mohamed, Amal M, Gad, Yehia Z, Abdelhak, Sonia, Hennig, Branwen J, Ramesar, Raj S, Landouré, Guida, Gaye, Amadou, Newport, Melanie J, Williams, Scott M, Ramsay, Michèle

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Validation and development of MTH1 inhibitors for treatment of cancer von Warpman Berglund, U., Sanjiv, K., Gad, H., Kalderén, C., Koolmeister, T., Pham, T., Gokturk, C., Jafari, R., Maddalo, G., Seashore-Ludlow, B., Chernobrovkin, A., Manoilov, A., Pateras, I.S., Rasti, A., Jemth, A.-S., Almlöf, I., Loseva, O., Visnes, T., Einarsdottir, B.O., Gaugaz, F.Z., Saleh, A., Platzack, B., Wallner, O.A., Vallin, K.S.A., Henriksson, M., Wakchaure, P., Borhade, S., Herr, P., Kallberg, Y., Baranczewski, P., Homan, E.J., Wiita, E., Nagpal, V., Meijer, T., Schipper, N., Rudd, S.G., Bräutigam, L., Lindqvist, A., Filppula, A., Lee, T.-C., Artursson, P., Nilsson, J.A., Gorgoulis, V.G., Lehtiö, J., Zubarev, R.A., Scobie, M., Helleday, T.

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