Spectrum of mutations in the ANTXR2 (CMG2) gene in infantile systemic hyalinosis and juvenile hyaline fibromatosis
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.
Published in British journal of dermatology (1951) (01.07.2010)
Published in British journal of dermatology (1951) (01.07.2010)
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Screening of Genital Anomalies in Newborns and Infants in Two Egyptian Governorates
Mazen, I., El-Ruby, M., Kamal, R., El-Nekhely, I., El-Ghandour, M., Tantawy, S., El-Gammal, M.
Published in Hormone research in paediatrics (01.01.2010)
Published in Hormone research in paediatrics (01.01.2010)
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Growth charts of Egyptian children with Down syndrome (0-36 months)
Meguid, N A, El-Kotoury, A I S, Abdel-Salam, G M H, El-Ruby, M O, Afifi, H H
Published in Eastern Mediterranean health journal (01.01.2004)
Published in Eastern Mediterranean health journal (01.01.2004)
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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
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.
Published in Sexual development (01.01.2013)
Published in Sexual development (01.01.2013)
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TERMINAL 2q DELETION AND PARTIAL TRISOMY CHROMOSOME 15q: A CLINICAL AND CYTOGENETIC STUDY
EL-BASSYOUNI, H. T, EL-GERZAWY, A. M. S, MOHAMED, A. M, KAMEL, A. K, HUSSEIN, H. A, THOMAS, M. M, EL-RUBY, M
Published in Genetic counseling (01.01.2014)
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Published in Genetic counseling (01.01.2014)
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Phenotypic and cytogenetic spectrum of 9p trisomy
Temtamy, S A, Kamel, A K, Ismail, S, Helmy, N A, Aglan, M S, El Gammal, M, El Ruby, M, Mohamed, A M
Published in Genetic counseling (2007)
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Published in Genetic counseling (2007)
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Emanuel syndrome due to unusual segregation of paternal origin
Zaki, M S, Mohamed, A M, Kamel, A K, El-Gerzawy, A M S, El-Ruby, M O
Published in Genetic counseling (01.01.2012)
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Published in Genetic counseling (01.01.2012)
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The most encountered groups of genetic disorders in Giza Governorate, Egypt
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
Published in Bratislavské lékarské listy (2010)
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Published in Bratislavské lékarské listy (2010)
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RING CHROMOSOME 15: EXPANDING THE PHENOTYPE
EID, M. M, EL-BASSYOUNI, H. T, EID, O. M, HAMAD, S. A, ELGERZAWY, A, ZAKI, M. S, EL-RUBY, M
Published in Genetic counseling (01.01.2013)
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Published in Genetic counseling (01.01.2013)
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Spectrum of mutations in the ANTXR2 ( CMG2 ) gene in infantile systemic hyalinosis and juvenile hyaline fibromatosis: Correspondence
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.
Published in British journal of dermatology (1951) (01.07.2010)
Published in British journal of dermatology (1951) (01.07.2010)
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New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects
Fayez, Alaaeldin G., Esmaiel, Nora N., Ashaat, Engy A., Refeat, Miral M., Lotfy, Randa S., Raouf, Haiam Abdel, El Ruby, Mona O.
Published in Journal of Taibah University Medical Sciences (01.12.2023)
Published in Journal of Taibah University Medical Sciences (01.12.2023)
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Klinefelter syndrome, rare variant 49, XXXXY
Salman, H, Abanamy, A, Khan, N, Basset, G, Choudhury, A H, El-Ruby, M O
Published in Annals of Saudi medicine (01.05.1991)
Published in Annals of Saudi medicine (01.05.1991)
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