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

Year Number of Results
1995 3
1996 1
1998 1
1999 1
2000 1
2001 2
2003 1
2004 1
2008 1
2009 1
2016 1
2024 0

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14 results

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Page 1
Prenatal diagnosis of Smith-Lemli-Opitz syndrome.
McGaughran JM, Clayton PT, Mills KA, Rimmer S, Moore L, Donnai D. McGaughran JM, et al. Am J Med Genet. 1995 Apr 10;56(3):269-71. doi: 10.1002/ajmg.1320560306. Am J Med Genet. 1995. PMID: 7778587
Biliary atresia in Kabuki syndrome.
McGaughran JM, Donnai D, Clayton-Smith J. McGaughran JM, et al. Am J Med Genet. 2000 Mar 13;91(2):157-8. Am J Med Genet. 2000. PMID: 10748418 No abstract available.
Interstitial deletion of 3p22.2-p24.2: the first reported case.
Liu HX, Oei PT, Mitchell EA, McGaughran JM. Liu HX, et al. Among authors: mcgaughran jm. J Med Genet. 2001 May;38(5):349-51. doi: 10.1136/jmg.38.5.349. J Med Genet. 2001. PMID: 11403048 Free PMC article. No abstract available.
Hereditary pancreatitis in a family of Aboriginal descent.
McGaughran JM, Kimble R, Upton J, George P. McGaughran JM, et al. J Paediatr Child Health. 2004 Aug;40(8):487-9. doi: 10.1111/j.1440-1754.2004.00437.x. J Paediatr Child Health. 2004. PMID: 15265195
14 results