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X
AbuDheim, Nada
8  Ergebnisse:
Personensuche X
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1

GM2 gangliosidosis in Saudi Arabia: Multiple mutations and ..:

Kaya, Namik ; Owain, Mohammad Al‐ ; AbuDheim, Nada...
American Journal of Medical Genetics Part A.  155 (2011)  6 - p. 1281-1284 , 2011
Link: https://doi.org/10.1002/..
 
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2

Genomic and transcriptomic analyses distinguish classic Ret..:

Colak, Dilek ; Al-Dhalaan, Hesham ; Nester, Michael...
Genomics.  97 (2011)  1 - p. 19-28 , 2011
Link: https://doi.org/10.1016/..
 
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3

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorp..:

Al-Zahrani, Jawaher ; Al-Dosari, Naji ; AbuDheim, Nada...
Molecular Cytogenetics.  4 (2011)  1 - p. , 2011
Link: https://doi.org/10.1186/..
 
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4

A novel interstitial microdeletion of 7q22.1‐7q22.3 detecte..:

Al‐Hassnan, Zuhair N. ; Al‐Bakheet, AlBandary ; Abu‐Dheim, Nada...
American Journal of Medical Genetics Part A.  155 (2011)  12 - p. 3128-3131 , 2011
Link: https://doi.org/10.1002/..
 
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5

A novel X-linked disorder with developmental delay and auti..:

Kaya, Namik ; Colak, Dilek ; Albakheet, Albandary...
Annals of Neurology.  71 (2011)  4 - p. 498-508 , 2011
Link: https://doi.org/10.1002/..
 
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6

A novel deletion of theMEN1gene in a large family of multip..:

Raef, Hussein ; Zou, Minjing ; Baitei, Essa Y....
Clinical Endocrinology.  75 (2011)  6 - p. 791-800 , 2011
Link: https://doi.org/10.1111/..
 
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7

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorp..:

Al-Zahrani, Jawaher ; Al-Dosari, Naji ; AbuDheim, Nada...
http://www.molecularcytogenetics.org/content/4/1/9.  , 2011
Link: http://www.molecularcyto..
 
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8

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorp..:

Sakati Nadia ; Al-Odaib Ali ; Al-Habit Ola...
http://www.molecularcytogenetics.org/content/4/1/9.  , 2011
Link: https://doi.org/10.1186/..
 
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