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Results by year

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

Year Number of Results
1969 2
1979 3
1980 2
1981 1
1982 2
1983 3
1984 3
1985 1
1986 1
1987 2
1988 4
1989 3
1990 9
1991 6
1992 9
1993 1
1996 2
1997 1
1998 3
2000 2
2001 2
2002 3
2003 6
2004 4
2005 7
2006 3
2007 12
2008 1
2009 1
2010 2
2011 1
2013 1
2015 1
2016 1
2024 0

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103 results

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Page 1
Restrictive dermopathy.
Gillerot Y, Koulischer L. Gillerot Y, et al. Am J Med Genet. 1987 May;27(1):239-40. doi: 10.1002/ajmg.1320270131. Am J Med Genet. 1987. PMID: 3605203 No abstract available.
The Baller-Gerold syndrome.
Van Maldergem L, Verloes A, Lejeune L, Gillerot Y. Van Maldergem L, et al. Among authors: gillerot y. J Med Genet. 1992 Apr;29(4):266-8. doi: 10.1136/jmg.29.4.266. J Med Genet. 1992. PMID: 1583650 Free PMC article.
Prenatal diagnosis of trisomy 6 mosaicism.
Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y. Destree A, et al. Among authors: gillerot y. Prenat Diagn. 2005 May;25(5):354-7. doi: 10.1002/pd.1149. Prenat Diagn. 2005. PMID: 15906424 Review.
The Marshall-Smith syndrome.
Charon A, Gillerot Y, Van Maldergem L, Van Schaftingen MH, de Bont B, Koulischer L. Charon A, et al. Among authors: gillerot y. Eur J Pediatr. 1990 Nov;150(1):54-5. doi: 10.1007/BF01959481. Eur J Pediatr. 1990. PMID: 2079077
Oro-facial-digital syndrome II.
Gillerot Y, Koulischer L. Gillerot Y, et al. Clin Genet. 1988 Feb;33(2):141-2. doi: 10.1111/j.1399-0004.1988.tb03426.x. Clin Genet. 1988. PMID: 3359665 No abstract available.
Deletion and point mutations of PTHLH cause brachydactyly type E.
Klopocki E, Hennig BP, Dathe K, Koll R, de Ravel T, Baten E, Blom E, Gillerot Y, Weigel JF, Krüger G, Hiort O, Seemann P, Mundlos S. Klopocki E, et al. Among authors: gillerot y. Am J Hum Genet. 2010 Mar 12;86(3):434-9. doi: 10.1016/j.ajhg.2010.01.023. Epub 2010 Feb 18. Am J Hum Genet. 2010. PMID: 20170896 Free PMC article.
103 results