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

Year Number of Results
1965 1
1967 2
1968 3
1969 2
1970 1
1971 2
1973 3
1974 2
1975 2
1976 2
1977 1
1978 3
1979 1
1980 1
1981 2
1982 1
1983 2
1984 3
1986 2
1988 1
1989 2
1990 3
1991 2
1992 7
1994 2
1995 1
1996 3
1997 3
1998 1
1999 4
2000 1
2001 3
2024 0

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68 results

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Page 1
[Maternal phenylketonuria].
Rittinger O, Plöchl E, Jarosch E. Rittinger O, et al. Among authors: plochl e. Padiatr Padol. 1984;19(1):87-92. Padiatr Padol. 1984. PMID: 6701000 German.
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III.
Lüdecke HJ, Schaper J, Meinecke P, Momeni P, Gross S, von Holtum D, Hirche H, Abramowicz MJ, Albrecht B, Apacik C, Christen HJ, Claussen U, Devriendt K, Fastnacht E, Forderer A, Friedrich U, Goodship TH, Greiwe M, Hamm H, Hennekam RC, Hinkel GK, Hoeltzenbein M, Kayserili H, Majewski F, Mathieu M, McLeod R, Midro AT, Moog U, Nagai T, Niikawa N, Orstavik KH, Plöchl E, Seitz C, Schmidtke J, Tranebjaerg L, Tsukahara M, Wittwer B, Zabel B, Gillessen-Kaesbach G, Horsthemke B. Lüdecke HJ, et al. Among authors: plochl e. Am J Hum Genet. 2001 Jan;68(1):81-91. doi: 10.1086/316926. Epub 2000 Dec 7. Am J Hum Genet. 2001. PMID: 11112658 Free PMC article.
[The intermediate form of maple syrup disease].
Rittinger O, Bachmann C, Irnberger T, Pilz P, Walter GF, Wendel U, Plöchl E. Rittinger O, et al. Among authors: plochl e. Klin Padiatr. 1986 Jan-Feb;198(1):37-43. doi: 10.1055/s-2008-1026850. Klin Padiatr. 1986. PMID: 3959487 German.
Clinical, cytogenetic and molecular analysis of three 46,XX males.
Plöchl E, Vlasak I, Rittinger O, Bergendi E, Stopar M, Kurnik P, Nachtigall M, Zierler H, Rappold GA, Schiebel K. Plöchl E, et al. J Pediatr Endocrinol Metab. 1999 May-Jun;12(3):389-95. doi: 10.1515/jpem.1999.12.3.389. J Pediatr Endocrinol Metab. 1999. PMID: 10821218
68 results