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

Year Number of Results
1970 1
1977 1
1979 1
1988 1
1989 1
1990 1
1993 2
1994 2
1995 4
1996 3
1997 2
1998 2
1999 3
2000 3
2001 4
2002 1
2003 1
2004 1
2005 2
2024 0

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PubMed (OMIM) for id: 339002

35 results

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Page 1
PAX2 gene mutation in a family with isolated renal hypoplasia.
Nishimoto K, Iijima K, Shirakawa T, Kitagawa K, Satomura K, Nakamura H, Yoshikawa N. Nishimoto K, et al. J Am Soc Nephrol. 2001 Aug;12(8):1769-1772. doi: 10.1681/ASN.V1281769. J Am Soc Nephrol. 2001. PMID: 11461952
Expression of the PAX2 gene in human embryos and exclusion in the CHARGE syndrome.
Tellier AL, Amiel J, Delezoide AL, Audollent S, Augé J, Esnault D, Encha-Razavi F, Munnich A, Lyonnet S, Vekemans M, Attié-Bitach T. Tellier AL, et al. Am J Med Genet. 2000 Jul 17;93(2):85-8. doi: 10.1002/1096-8628(20000717)93:2<85::aid-ajmg1>3.0.co;2-b. Am J Med Genet. 2000. PMID: 10869107
35 results