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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
1994 1
1995 3
1996 4
1997 2
1999 1
2000 1
2002 1
2003 2
2011 1
2012 1
2013 1
2016 2
2017 1
2020 1
2024 0

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22 results

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Page 1
Characterizing the morbid genome of ciliopathies.
Shaheen R, Szymanska K, Basu B, Patel N, Ewida N, Faqeih E, Al Hashem A, Derar N, Alsharif H, Aldahmesh MA, Alazami AM, Hashem M, Ibrahim N, Abdulwahab FM, Sonbul R, Alkuraya H, Alnemer M, Al Tala S, Al-Husain M, Morsy H, Seidahmed MZ, Meriki N, Al-Owain M, AlShahwan S, Tabarki B, Salih MA; Ciliopathy WorkingGroup; Faquih T, El-Kalioby M, Ueffing M, Boldt K, Logan CV, Parry DA, Al Tassan N, Monies D, Megarbane A, Abouelhoda M, Halees A, Johnson CA, Alkuraya FS. Shaheen R, et al. Among authors: al husain m. Genome Biol. 2016 Nov 28;17(1):242. doi: 10.1186/s13059-016-1099-5. Genome Biol. 2016. PMID: 27894351 Free PMC article.
Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.
Anazi S, Maddirevula S, Faqeih E, Alsedairy H, Alzahrani F, Shamseldin HE, Patel N, Hashem M, Ibrahim N, Abdulwahab F, Ewida N, Alsaif HS, Al Sharif H, Alamoudi W, Kentab A, Bashiri FA, Alnaser M, AlWadei AH, Alfadhel M, Eyaid W, Hashem A, Al Asmari A, Saleh MM, AlSaman A, Alhasan KA, Alsughayir M, Al Shammari M, Mahmoud A, Al-Hassnan ZN, Al-Husain M, Osama Khalil R, Abd El Meguid N, Masri A, Ali R, Ben-Omran T, El Fishway P, Hashish A, Ercan Sencicek A, State M, Alazami AM, Salih MA, Altassan N, Arold ST, Abouelhoda M, Wakil SM, Monies D, Shaheen R, Alkuraya FS. Anazi S, et al. Among authors: al husain m. Mol Psychiatry. 2017 Apr;22(4):615-624. doi: 10.1038/mp.2016.113. Epub 2016 Jul 19. Mol Psychiatry. 2017. PMID: 27431290
Schwartz-Jampel syndrome in Saudi children.
Al-Husain MA, Al-Eissa YA, Al-Sohaibani MO, Al-Omair AO, Al-Nasser MN. Al-Husain MA, et al. Ann Saudi Med. 1994 Mar;14(2):152-6. doi: 10.5144/0256-4947.1994.152. Ann Saudi Med. 1994. PMID: 17589085 Free article. No abstract available.
Down's syndrome in Saudi Arabia: incidence and cytogenetics.
Niazi MA, al-Mazyad AS, al-Husain MA, al-Mofada SM, al-Zamil FA, Khashoggi TY, al-Eissa YA. Niazi MA, et al. Among authors: al husain ma. Hum Hered. 1995 Mar-Apr;45(2):65-9. doi: 10.1159/000154261. Hum Hered. 1995. PMID: 7750976
Classification of hand anomalies in Apert's syndrome.
al-Qattan MM, al-Husain MA. al-Qattan MM, et al. Among authors: al husain ma. J Hand Surg Br. 1996 Apr;21(2):266-8. doi: 10.1016/s0266-7681(96)80113-6. J Hand Surg Br. 1996. PMID: 8732416
POC1A truncation mutation causes a ciliopathy in humans characterized by primordial dwarfism.
Shaheen R, Faqeih E, Shamseldin HE, Noche RR, Sunker A, Alshammari MJ, Al-Sheddi T, Adly N, Al-Dosari MS, Megason SG, Al-Husain M, Al-Mohanna F, Alkuraya FS. Shaheen R, et al. Among authors: al husain m. Am J Hum Genet. 2012 Aug 10;91(2):330-6. doi: 10.1016/j.ajhg.2012.05.025. Epub 2012 Jul 26. Am J Hum Genet. 2012. PMID: 22840364 Free PMC article.
22 results