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Gaboon, Nagwa E.A
9  Ergebnisse:
Artikel (Online) X
Personensuche X
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1

A Novel Homozygous Frameshift Variant in DYM Causing Dyggve..:

Gaboon, Nagwa E. A. ; Parveen, Asia ; Ahmad, Khaled A....
Frontiers in Pediatrics.  8 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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2

Exome sequencing and metabolomic analysis of a chronic kidn..:

Gaboon, Nagwa E.A. ; Banaganapalli, Babajan ; Nasser, Khalidah...
Saudi Journal of Biological Sciences.  27 (2020)  1 - p. 324-334 , 2020
Link: https://doi.org/10.1016/..
 
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3

A Novel Homozygous Frameshift Mutation in CCN6 Causing Prog..:

Gaboon, Nagwa E. A. ; Parveen, Asia ; El Beheiry, Ahmed...
Frontiers in Pediatrics.  7 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
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4

Deleterious Variants in WNT10A, EDAR, and EDA Causing Isola..:

Parveen, Asia ; Khan, Sher Alam ; Mirza, Muhammad Usman...
International Journal of Molecular Sciences.  20 (2019)  21 - p. 5282 , 2019
Link: https://doi.org/10.3390/..
 
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5

Case of Sjögren–Larsson syndrome with a large deletion in t..:

Gaboon, Nagwa E. A. ; Jelani, Musharraf ; Almramhi, Mona M...
The Journal of Dermatology.  42 (2015)  7 - p. 706-709 , 2015
Link: https://doi.org/10.1111/..
 
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6

Hereditary periodic fever syndromes:

Shawky, Rabah M. ; Gaboon, Nagwa E.A.
Egyptian Journal of Medical Human Genetics.  12 (2011)  2 - p. 117-125 , 2011
Link: https://doi.org/10.1016/..
 
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7

Nutritional genomics and personalized diet:

Gaboon, Nagwa E.A.
Egyptian Journal of Medical Human Genetics.  12 (2011)  1 - p. 1-7 , 2011
Link: https://doi.org/10.1016/..
 
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8

Genetic etiology and clinical challenges of phenylketonuria:

Elhawary, Nasser A. ; AlJahdali, Imad A. ; Abumansour, Iman S....
Human Genomics.  16 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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9

Multiple pterygium syndrome with marked pterygia of the fin..:

Shawky, Rabah M. ; Elsayed, Solaf ; Gaboon, Nagwa
Egyptian Journal of Medical Human Genetics.  13 (2012)  1 - p. 107-113 , 2012
Link: https://doi.org/10.1016/..
 
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