El-Ruby MO - Search Results

1

Growth charts of Egyptian children with Down syndrome (0-36 months).

Meguid NA, El-Kotoury AI, Abdel-Salam GM, El-Ruby MO, Afifi HH. Meguid NA, et al. East Mediterr Health J. 2004 Jan-Mar;10(1-2):106-15. East Mediterr Health J. 2004. PMID: 16201715 Free article.

2

Assessment of pubertal development in Egyptian girls.

Hosny LA, El-Ruby MO, Zaki ME, Aglan MS, Zaki MS, El Gammal MA, Mazen IM. Hosny LA, et al. J Pediatr Endocrinol Metab. 2005 Jun;18(6):577-84. doi: 10.1515/jpem.2005.18.6.577. J Pediatr Endocrinol Metab. 2005. PMID: 16042325

3

Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.

Zaki MS, Kamel AA, El-Ruby M. Zaki MS, et al. Genet Couns. 2005;16(4):393-402. Genet Couns. 2005. PMID: 16440882

4

Spectrum of mutations in the ANTXR2 (CMG2) gene in infantile systemic hyalinosis and juvenile hyaline fibromatosis.

El-Kamah GY, Fong K, El-Ruby M, Afifi HH, Clements SE, Lai-Cheong JE, Amr K, El-Darouti M, McGrath JA. El-Kamah GY, et al. Br J Dermatol. 2010 Jul;163(1):213-5. doi: 10.1111/j.1365-2133.2010.09769.x. Epub 2010 Mar 17. Br J Dermatol. 2010. PMID: 20331448 No abstract available.

5

The most encountered groups of genetic disorders in Giza Governorate, Egypt.

Afifi HH, El-Ruby MO, El-Bassyouni HT, Ismail SI, Aglan MS, El-Harouni AA, Mazen IM, Zaki MS, Bassiouni RI, Hosny LA, El-Kamah GY, El-Kotoury AI, Ashour AM, Abdel-Salam GM, El-Gammal MA, Hamed K, Kamal RM, El-Nekhely I, Temtamy SA. Afifi HH, et al. Bratisl Lek Listy. 2010;111(2):62-9. Bratisl Lek Listy. 2010. PMID: 20429316

6

Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype.

Abdel-Salam GM, Flores-Sarnat L, El-Ruby MO, Parboosingh J, Bridge P, Eid MM, El-Badry TH, Effat L, Curatolo P, Temtamy SA. Abdel-Salam GM, et al. Am J Med Genet A. 2011 Jan;155A(1):207-14. doi: 10.1002/ajmg.a.33777. Am J Med Genet A. 2011. PMID: 21204234

7

A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION.

Eid MO, Eid MM, Kamel AK, El-Ruby M, Abdel-Salam GM. Eid MO, et al. Genet Couns. 2015;26(2):153-61. Genet Couns. 2015. PMID: 26349184

8

Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2.

El-Ruby M, El-Din Fayez A, El-Dessouky SH, Aglan MS, Mazen I, Ismail N, Afifi HH, Eid MM, Mostafa MI, Mehrez MI, Khalil Y, Zaki MS, Gaber KR, Abdel-Hamid MS, Abdel-Salam GMH. El-Ruby M, et al. Am J Med Genet A. 2018 May;176(5):1190-1194. doi: 10.1002/ajmg.a.38655. Am J Med Genet A. 2018. PMID: 29681084

9

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.

Mohamed AM, Kamel AK, Eid MM, Eid OM, Mekkawy M, Hussein SH, Zaki MS, Esmail S, Afifi HH, El-Kamah GY, Otaify GA, El-Awady HA, Elaidy A, Essa MY, El-Ruby M, Ashaat EA, Hammad SA, Mazen I, Abdel-Salam GMH, Aglan M, Temtamy S. Mohamed AM, et al. Mol Genet Genomic Med. 2021 Nov;9(11):e1829. doi: 10.1002/mgg3.1829. Epub 2021 Oct 5. Mol Genet Genomic Med. 2021. PMID: 34609792 Free PMC article.

10

Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.

El-Ruby M, Hemly NA, Zaki MS. El-Ruby M, et al. Genet Couns. 2007;18(2):217-26. Genet Couns. 2007. PMID: 17710874

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