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

Year Number of Results
1988 1
1989 9
1990 1
1991 4
1992 2
1994 1
1996 1
2010 1
2018 1
2024 0

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Page 1
Nonsyndromal microphthalmia.
Teebi AS, AL-Saleh QA. Teebi AS, et al. Among authors: al saleh qa. Clin Genet. 1989 Apr;35(4):311-2. doi: 10.1111/j.1399-0004.1989.tb02950.x. Clin Genet. 1989. PMID: 2714018 No abstract available.
Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait.
Nanda A, Liu L, Al-Ajmi H, Al-Saleh QA, Al-Fadhli S, Anim JT, Ozoemena L, Mellerio JE, McGrath JA. Nanda A, et al. Among authors: al saleh qa. Int J Dermatol. 2018 Sep;57(9):1058-1067. doi: 10.1111/ijd.14099. Epub 2018 Jul 16. Int J Dermatol. 2018. PMID: 30011071
New autosomal recessive faciodigitogenital syndrome.
Teebi AS, Naguib KK, Al-Awadi S, Al-Saleh QA. Teebi AS, et al. Among authors: al saleh qa. J Med Genet. 1988 Jun;25(6):400-6. doi: 10.1136/jmg.25.6.400. J Med Genet. 1988. PMID: 3398008 Free PMC article.
A multicenter therapeutic study of 1100 children with brucellosis.
Lubani MM, Dudin KI, Sharda DC, Ndhar DS, Araj GF, Hafez HA, al-Saleh QA, Helin I, Salhi MM. Lubani MM, et al. Among authors: al saleh qa. Pediatr Infect Dis J. 1989 Feb;8(2):75-8. Pediatr Infect Dis J. 1989. PMID: 2649867 Clinical Trial.
Meckel syndrome and neural tube defects in Kuwait.
Teebi AS, al Saleh QA, Odeh H. Teebi AS, et al. Among authors: al saleh qa. J Med Genet. 1992 Feb;29(2):140. doi: 10.1136/jmg.29.2.140-a. J Med Genet. 1992. PMID: 1613765 Free PMC article. No abstract available.
21 results