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Author/Creator Hariri, Hadla

1. Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis. Issue 3 (December 2018)

Authors:
Hariri, Hadla; Kurban, Mazen; Al-Haddad, Christiane; Fahed, Akl C.; Poladian, Sarin; Khalil, Athar; Abbas, Oussama; Arabi, Mariam; Bitar, Fadi; Nemer, Georges
Journal:
Journal of dermatological science
Issue:
Volume 92:Issue 3(2018)
Page Start:
237
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient. Issue 2 (20th December 2015)

Authors:
Kassab, Kameel; Hariri, Hadla; Gharibeh, Lara; Fahed, Akl C.; Zein, Manal; El‐Rassy, Inaam; Nemer, Mona; El‐Rassi, Issam; Bitar, Fadi; Nemer, Georges
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 4:Issue 2(2016)
Page Start:
160
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗