Ich stimme zu, dass diese Seite Cookies verwende. Weitere Informationen finden Sie unter unseren Datenschutzerklärungen .
X
Mohamed, Jawahir Y.
6  Ergebnisse:
OpenAccess-Volltexte X
Personensuche X
?
1

Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocatio..:

Patel, Nisha ; Khan, Arif O ; Mansour, Ahmad...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC.  , 2014
Link: http://www.ncbi.nlm.nih...
 
?
2

Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause K..:

Mohamed, Jawahir Y ; Faqeih, Eissa ; Alsiddiky, Abdulmonem...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542464.  , 2013
Link: http://www.ncbi.nlm.nih...
 
?
3

Mutations in LRPAP1 Are Associated with Severe Myopia in Hu..:

Aldahmesh, Mohammed A ; Khan, Arif O ; Alkuraya, Hisham...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738831.  , 2013
Link: http://www.ncbi.nlm.nih...
 
?
4

In search of triallelism in Bardet–Biedl syndrome:

Abu-Safieh, Leen ; Al-Anazi, Shamsa ; Al-Abdi, Lama...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306854.  , 2012
Link: http://www.ncbi.nlm.nih...
 
?
5

Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectua..:

Aldahmesh, Mohammed A ; Mohamed, Jawahir Y ; Alkuraya, Hisham S...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234380.  , 2011
Link: http://www.ncbi.nlm.nih...
 
?
6

Accelerating Novel Candidate Gene Discovery in Neurogenetic..:

Anas M. Alazami ; Nisha Patel ; Hanan E. Shamseldin...
http://www.sciencedirect.com/science/article/pii/S2211124714010444.  , 2015
Link: https://doi.org/10.1016/..
 
1-6