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Results by year

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

Year Number of Results
1971 4
1972 4
1973 5
1974 3
1975 8
1976 17
1977 15
1978 21
1979 13
1980 12
1981 9
1982 11
1983 10
1984 9
1985 15
1986 27
1987 18
1988 18
1989 24
1990 21
1991 21
1992 26
1993 24
1994 20
1995 27
1996 14
1997 18
1998 20
1999 13
2000 6
2001 10
2002 4
2004 2
2005 4
2006 5
2007 5
2008 5
2009 6
2010 4
2011 7
2012 6
2013 6
2016 2
2017 1
2018 1
2019 1
2020 2
2024 0

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Search Results

516 results

Results by year

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Page 1
Genetic heterogeneity in Laron syndrome.
Francke U, Berg MA. Francke U, et al. Acta Paediatr Suppl. 1993 Sep;82 Suppl 391:3-7; discussion 8. doi: 10.1111/j.1651-2227.1993.tb12916.x. Acta Paediatr Suppl. 1993. PMID: 8219474 Review. No abstract available.
Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics.
Bieber FR, Cherry AM, Emanuel BS, Francke U, Hoyme HE, Jackson LG, Morton CC, Muenke M, Powell CM, Punnett HH, Rao PN, Schwartz S, Stevenson RE, Van Dyke DL. Bieber FR, et al. Among authors: francke u. Genet Med. 2017 Mar;19(3):294-296. doi: 10.1038/gim.2016.171. Epub 2016 Nov 17. Genet Med. 2017. PMID: 27854359 Free article.
Growth hormone receptor deficiency in Ecuador.
Rosenbloom AL, Guevara-Aguirre J, Rosenfeld RG, Francke U. Rosenbloom AL, et al. Among authors: francke u. J Clin Endocrinol Metab. 1999 Dec;84(12):4436-43. doi: 10.1210/jcem.84.12.6283. J Clin Endocrinol Metab. 1999. PMID: 10599699 Review. No abstract available.
Imprinted genes in the Prader-Willi deletion.
Francke U. Francke U. Novartis Found Symp. 1998;214:264-75; discussion 275-9. doi: 10.1002/9780470515501.ch16. Novartis Found Symp. 1998. PMID: 9601023 Review.
Cytogenetic analysis in melanoma and nevi.
Cowan JM, Francke U. Cowan JM, et al. Among authors: francke u. Cancer Treat Res. 1991;54:3-16. doi: 10.1007/978-1-4615-3938-4_1. Cancer Treat Res. 1991. PMID: 1673858 Review.
The pallister mosaic syndrome.
Pallister PD, Meisner LF, Elejalde BR, Francke U, Herrmann J, Spranger J, Tiddy W, Inhorn SL, Opitz JM. Pallister PD, et al. Among authors: francke u. Birth Defects Orig Artic Ser. 1977;13(3B):103-110. Birth Defects Orig Artic Ser. 1977. PMID: 890087 No abstract available.
The penta-X syndrome.
Monheit A, Francke U, Saunders B, Jones KL. Monheit A, et al. Among authors: francke u. J Med Genet. 1980 Oct;17(5):392-6. doi: 10.1136/jmg.17.5.392. J Med Genet. 1980. PMID: 7218280 Free PMC article.
516 results