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Author/Creator Ashaat, Engy A.

1. Blepharophimosis‐ptosis‐intellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum. Issue 12 (19th September 2020)

Authors:
Zaki, Maha S.; Otaify, Ghada A.; Ismail, Samira; Issa, Mahmoud Y.; El‐Ruby, Mona O.; Sadek, Abdelrahim A.; Ashaat, Engy A.; El Saeidi, Sonia A.; Aglan, Mona S.; Temtamy, Samia; Abdel‐Hamid, Mohamed S.
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 12(2020)
Page Start:
2857
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 genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature. Issue 2 (20th November 2020)

Authors:
Mekkawy, Mona K.; Kamel, Alaa K.; Thomas, Manal M.; Ashaat, Engy A.; Zaki, Maha S.; Eid, Ola M.; Ismail, Samira; Hammad, Saida A.; Megahed, Hisham; ElAwady, Heba; Refaat, Khaled M.; Hussien, Shymaa; Helmy, Nivine; Abd Allah, Sally G.; Mohamed, Amal M.; El Ruby, Mona O.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 2(2021)
Page Start:
n/a
Record Type:
Journal Article
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4. Cover Image, Volume 176A, Number 5, May 2018. Issue 5 (21st April 2018)

Authors:
Kruszka, Paul; Porras, Antonio R.; de Souza, Deise Helena; Moresco, Angélica; Huckstadt, Victoria; Gill, Ashleigh D.; Boyle, Alec P.; Hu, Tommy; Addissie, Yonit A.; Mok, Gary T. K.; Tekendo‐Ngongang, Cedrik; Fieggen, Karen; Prijoles, Eloise J.; Tanpaiboon, Pranoot; Honey, Engela; Luk, Ho‐Ming; Lo...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 5(2018)
Page Start:
n/a
Record Type:
Journal Article
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5. Rubinstein–Taybi syndrome in diverse populations. Issue 12 (27th September 2020)

Authors:
Tekendo‐Ngongang, Cedrik; Owosela, Babajide; Fleischer, Nicole; Addissie, Yonit A.; Malonga, Bryan; Badoe, Ebenezer; Gupta, Neerja; Moresco, Angélica; Huckstadt, Victoria; Ashaat, Engy A.; Hussen, Dalia Farouk; Luk, Ho‐Ming; Lo, Ivan F. M.; Hon‐Yin Chung, Brian; Fung, Jasmine L. F.; Moretti‐Ferre...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 12(2020)
Page Start:
2939
Record Type:
Journal Article
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7. Turner syndrome in diverse populations. Issue 2 (19th December 2019)

Authors:
Kruszka, Paul; Addissie, Yonit A.; Tekendo‐Ngongang, Cedrik; Jones, Kelly L.; Savage, Sarah K.; Gupta, Neerja; Sirisena, Nirmala D.; Dissanayake, Vajira H. W.; Paththinige, C. Sampath; Aravena, Teresa; Nampoothiri, Sheela; Yesodharan, Dhanya; Girisha, Katta M.; Patil, Siddaramappa Jagdish; Jamuar...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 2(2020)
Page Start:
303
Record Type:
Journal Article
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8. Williams–Beuren syndrome in diverse populations. Issue 5 (21st April 2018)

Authors:
Kruszka, Paul; Porras, Antonio R.; de Souza, Deise Helena; Moresco, Angélica; Huckstadt, Victoria; Gill, Ashleigh D.; Boyle, Alec P.; Hu, Tommy; Addissie, Yonit A.; Mok, Gary T. K.; Tekendo‐Ngongang, Cedrik; Fieggen, Karen; Prijoles, Eloise J.; Tanpaiboon, Pranoot; Honey, Engela; Luk, Ho‐Ming; Lo...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 5(2018)
Page Start:
1128
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗