الفهرسة نشطة
للباحثين للناشرين تسجيل الدخول إنشاء حساب
الرئيسية المؤلفون Radwa Gamal
RG

Radwa Gamal

h-3 H-Index
29 Citations
20 Papers

Published Papers

20 indexed
1
Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2016.10.001
8 citations 388
2
Meier-Gorlin syndrome: Report of an additional patient with congenital heart disease
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.04.003
6 citations 393
3
Meier–Gorlin syndrome: An additional Egyptian patient with gastroesophageal reflux, hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.12.006
4 citations 391
4
Bilateral iris, choroid, optic nerve colobomas and retinal detachment in an Egyptian patient with mild Baraitser–Winter syndrome
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2013.11.001
2 citations 391
5
Berardinelli–Seip syndrome type 2 – An Egyptian child
Egyptian Journal of Medical Human Genetics Q2 2015 10.1016/j.ejmhg.2014.08.004
2 citations 384
6
Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2015.12.001
2 citations 390
7
Baraitser–Winter syndrome: An additional Egyptian patient with skeletal anomalies, bilateral iris and choroid colobomas, retinal hypoplasia and hypoplastic scrotum
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.04.004
1 citations 390
8
Christ-Siemens-Touraine syndrome with cleft palate, absent nipples, gallstones and mild mental retardation in an Egyptian child
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.06.002
1 citations 387
9
WITHDRAWN: Majewski Osteodysplastic Primordial Dwarfism, Type II with marked loss of subcutaneous fat, severe anemia, clenched hands and skeletal anomalies in an Egyptian patient
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2017.08.008
1 citations 390
10
REMOVED: An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2017.06.001
1 citations 390
11
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2017.04.002
1 citations 387
12
Oral–Facial–Digital Syndrome type VI with self mutilations
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.05.006
0 citations 391
13
Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child
Egyptian Journal of Medical Human Genetics Q2 2015 10.1016/j.ejmhg.2014.10.003
0 citations 383
14
Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient
Egyptian Journal of Medical Human Genetics Q2 2015 10.1016/j.ejmhg.2014.12.004
0 citations 384
15
Challenges in diagnosis and counseling of a family with two recessive neurometabolic disorders
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.12.005
0 citations 389
16
C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2016.01.006
0 citations 392
17
Progress in genetics of coronary artery disease
Egyptian Journal of Medical Human Genetics Q2 2018 10.1016/j.ejmhg.2017.11.001
0 citations 385
18
Cardiomyopathy in Vici syndrome
Egyptian Journal of Medical Human Genetics Q2 2018 10.1016/j.ejmhg.2017.12.003
0 citations 388
19
Cantu syndrome in an Egyptian child
Egyptian Journal of Medical Human Genetics Q2 2018 10.1016/j.ejmhg.2018.01.005
0 citations 389
20
Removal notice to “An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings” [Egypt J Med Hum Genet 18 (2017) 393–396]
Egyptian Journal of Medical Human Genetics Q2 2018 10.1016/j.ejmhg.2018.04.004
0 citations 386

Publication Activity

Journals Published In

Egyptian Journal of Medical Human Genetics
🇪🇬 Q2 AMS 99
Egyptian Journal of Medical Human Genetics
🇪🇬 Q2 AMS 98