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Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia. [electronic resource] by
- Kaya, Namik
- Colak, Dilek
- Al-Bakheet, Albandary
- Al-Younes, Banan
- Tulbah, Sahar
- Daghestani, Maha
- Al-Mutairi, Fuad
- Al-Amoudi, Mohammed
- Al-Odaib, Ali
- Al-Aqeel, Aida I
Producer: 20130419
In:
Gene vol. 513
Availability: No items available.
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7.
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ICF syndrome in Saudi Arabia: immunological, cytogenetic and molecular analysis. [electronic resource] by
- Kaya, Namik
- Al-Muhsen, Saleh
- Al-Saud, Bandar
- Al-Bakheet, Albandary
- Colak, Dilek
- Al-Ghonaium, Abdulaziz
- Al-Dhekri, Hasan
- Al-Mousa, Hamoud
- Arnaout, Rand
- Al-Owain, Mohammad
- Iqbal, Mohammad
Producer: 20110928
In:
Journal of clinical immunology vol. 31
Availability: No items available.
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8.
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First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient. [electronic resource] by
- Alsagob, Maysoon
- Salih, Mustafa A
- Hamad, Muddathir H A
- Al-Yafee, Yusra
- Al-Zahrani, Jawaher
- Al-Bakheet, Albandary
- Nester, Michael
- Sakati, Nadia
- Wakil, Salma M
- AlOdaib, Ali
- Colak, Dilek
- Kaya, Namik
Publication details: Molecular cytogenetics 2019
In:
Molecular cytogenetics vol. 12
Availability: No items available.
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9.
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Renal failure associated with APECED and terminal 4q deletion: evidence of autoimmune nephropathy. [electronic resource] by
- Al-Owain, Mohammed
- Kaya, Namik
- Al-Zaidan, Hamad
- Bin Hussain, Ibrahim
- Al-Manea, Hadeel
- Al-Hindi, Hindi
- Kennedy, Shelley
- Iqbal, M Anwar
- Al-Mojalli, Hamad
- Al-Bakheet, Albandary
- Puel, Anne
- Casanova, Jean-Laurent
- Al-Muhsen, Saleh
Producer: 20110621
In:
Clinical & developmental immunology vol. 2010
Availability: No items available.
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10.
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Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII. [electronic resource] by
- Kaya, Namik
- Aldhalaan, Hesham
- Al-Younes, Banan
- Colak, Dilek
- Shuaib, Taghreed
- Al-Mohaileb, Fahad
- Al-Sugair, Abdulaziz
- Nester, Michael
- Al-Yamani, Suad
- Al-Bakheet, Albandary
- Al-Hashmi, Nadia
- Al-Sayed, Moeen
- Meyer, Brian
- Jungbluth, Heinz
- Al-Owain, Mohammed
Producer: 20120117
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 156B
Availability: No items available.
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11.
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None [electronic resource] by
- Kaya, Namik
- Alsagob, Maysoon
- D'Adamo, Maria Cristina
- Al-Bakheet, Albandary
- Hasan, Sonia
- Muccioli, Maria
- Almutairi, Faten B
- Almass, Rawan
- Aldosary, Mazhor
- Monies, Dorota
- Mustafa, Osama M
- Alyounes, Banan
- Kenana, Rosan
- Al-Zahrani, Jawaher
- Naim, Eva
- Binhumaid, Faisal S
- Qari, Alya
- Almutairi, Fatema
- Meyer, Brian
- Plageman, Timothy F
- Pessia, Mauro
- Colak, Dilek
- Al-Owain, Mohammed
Publication details: Journal of medical genetics Nov 2016
In:
Journal of medical genetics vol. 53
Availability: No items available.
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12.
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Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways. [electronic resource] by
- Aldosary, Mazhor
- Al-Bakheet, AlBandary
- Al-Dhalaan, Hesham
- Almass, Rawan
- Alsagob, Maysoon
- Al-Younes, Banan
- AlQuait, Laila
- Mustafa, Osama Mufid
- Bulbul, Mustafa
- Rahbeeni, Zuhair
- Alfadhel, Majid
- Chedrawi, Aziza
- Al-Hassnan, Zuhair
- AlDosari, Mohammed
- Al-Zaidan, Hamad
- Al-Muhaizea, Mohammad A
- AlSayed, Moeenaldeen D
- Salih, Mustafa A
- AlShammari, Mai
- Faiyaz-Ul-Haque, Muhammad
- Chishti, Mohammad Azhar
- Al-Harazi, Olfat
- Al-Odaib, Ali
- Kaya, Namik
- Colak, Dilek
Producer: 20210430
In:
Omics : a journal of integrative biology vol. 24
Availability: No items available.
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