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Author/Creator El‐Ruby, Mona

1. Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development. Issue 6 (19th March 2021)

Authors:
Mazen, Inas; Mekkawy, Mona; Kamel, Alaa; Essawi, Mona; Hassan, Heba; Abdel‐Hamid, Mohamed; Amr, Khalda; Soliman, Hala; El‐Ruby, Mona; Torky, Ahmed; El Gammal, Mona; Elaidy, Aya; Bashamboo, Anu; McElreavey, Kenneth
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 6(2021)
Page Start:
1666
Record Type:
Journal Article
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2. Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly. Issue 11 (5th October 2021)

Authors:
Mohamed, Amal M.; Kamel, Alaa K.; Eid, Maha M.; Eid, Ola M.; Mekkawy, Mona; Hussein, Shymaa H.; Zaki, Maha S.; Esmail, Samira; Afifi, Hanan H.; El‐Kamah, Ghada Y.; Otaify, Ghada A.; El‐Awady, Heba Ahmed; Elaidy, Aya; Essa, Mahmoud Y.; El‐Ruby, Mona; Ashaat, Engy A.; Hammad, Saida A.; Mazen, Inas;...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 11(2021)
Page Start:
n/a
Record Type:
Journal Article
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3. Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations. (18th August 2015)

Authors:
Aglan, Mona; Amr, Khalda; Ismail, Samira; Ashour, Adel; Otaify, Ghada A.; Mehrez, Mennat Allah I.; Aboul‐Ezz, Eman H. A.; El‐Ruby, Mona; Mazen, Inas; Abdel‐Hamid, Mohamed S.; Temtamy, Samia A.
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 12(2015:Dec.)
Page Start:
3054
Record Type:
Journal Article
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4. Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type‐2. Issue 5 (21st April 2018)

Authors:
El‐Ruby, Mona; El‐Din Fayez, Alaa; El‐Dessouky, Sara H.; Aglan, Mona S.; Mazen, Inas; Ismail, Nora; Afifi, Hanan H.; Eid, Maha M.; Mostafa, Mostafa I.; Mehrez, Mennat I.; Khalil, Yasmin; Zaki, Maha S.; Gaber, Khaled R.; Abdel‐Hamid, Mohamed S.; Abdel‐Salam, Ghada M. H.
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 5(2018)
Page Start:
1190
Record Type:
Journal Article
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