Search

Author/Creator Thomas, Manal M.

1. 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
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. De Novo 17q24.2–q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features. (31st May 2015)

Authors:
Afifi, Hanan H.; Fukai, Ryoko; Miyake, Noriko; Gamal el Din, Amina A.; Eid, Maha M.; Eid, Ola M.; Thomas, Manal M.; El‐Badry, Tarek H.; Tosson, Angie M. S.; Abdel‐Salam, Ghada M. H.; Matsumoto, Naomichi
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 10(2015:Oct.)
Page Start:
2418
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. De Novo 17q24.2–q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features. (31st May 2015)

Authors:
Afifi, Hanan H.; Fukai, Ryoko; Miyake, Noriko; Gamal el Din, Amina A.; Eid, Maha M.; Eid, Ola M.; Thomas, Manal M.; El‐Badry, Tarek H.; Tosson, Angie M. S.; Abdel‐Salam, Ghada M. H.; Matsumoto, Naomichi
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 10(2015:Oct.)
Page Start:
2418
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗