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Results by year

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

Year Number of Results
1965 1
1978 1
1980 4
1981 6
1982 2
1983 2
1984 1
1985 1
1986 6
1987 5
1988 6
1989 6
1990 5
1991 4
1992 9
1993 3
1994 6
1995 5
1996 3
1997 5
1998 6
1999 7
2000 3
2001 1
2002 2
2003 3
2004 4
2005 3
2006 1
2007 1
2011 1
2012 1
2017 1
2024 0

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Search Results

114 results

Results by year

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Page 1
Waardenburg syndrome.
Read AP, Newton VE. Read AP, et al. J Med Genet. 1997 Aug;34(8):656-65. doi: 10.1136/jmg.34.8.656. J Med Genet. 1997. PMID: 9279758 Free PMC article. Review.
PAX genes.
Strachan T, Read AP. Strachan T, et al. Among authors: read ap. Curr Opin Genet Dev. 1994 Jun;4(3):427-38. doi: 10.1016/0959-437x(94)90032-9. Curr Opin Genet Dev. 1994. PMID: 7919921 Review.
Waardenburg syndrome.
Read AP. Read AP. Adv Otorhinolaryngol. 2000;56:32-8. doi: 10.1159/000059069. Adv Otorhinolaryngol. 2000. PMID: 10868211 Review. No abstract available.
How clinicians add to knowledge of development.
Donnai D, Read AP. Donnai D, et al. Among authors: read ap. Lancet. 2003 Aug 9;362(9382):477-84. doi: 10.1016/S0140-6736(03)14076-7. Lancet. 2003. PMID: 12927438 Review.
Beckwith-Wiedemann syndrome.
Norman AM, Read AP, Donnai D. Norman AM, et al. Among authors: read ap. J Med Genet. 1992 Sep;29(9):679. doi: 10.1136/jmg.29.9.679. J Med Genet. 1992. PMID: 1404305 Free PMC article. No abstract available.
Hypomelanosis of Ito.
Donnai D, Read AP. Donnai D, et al. Among authors: read ap. Lancet. 1992 Mar 28;339(8796):819-20. doi: 10.1016/0140-6736(92)91956-9. Lancet. 1992. PMID: 1347852 No abstract available.
114 results