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Results by year

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

Year Number of Results
1978 1
1980 2
1981 7
1983 4
1984 5
1985 4
1986 4
1987 6
1988 4
1989 5
1990 5
1991 6
1992 4
1993 11
1994 12
1995 14
1996 9
1997 12
1998 9
1999 4
2000 5
2001 2
2002 9
2003 7
2004 3
2005 5
2006 5
2007 7
2008 6
2009 5
2010 7
2011 3
2012 1
2013 1
2014 3
2015 2
2016 3
2017 3
2018 1
2019 3
2020 2
2021 3
2022 3
2023 2

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Search Results

210 results

Results by year

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Page 1
Dominance and homozygosity.
Zlotogora J. Zlotogora J. Am J Med Genet. 1997 Feb 11;68(4):412-6. doi: 10.1002/(sici)1096-8628(19970211)68:4<412::aid-ajmg8>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9021013 Review.
Germ line mosaicism.
Zlotogora J. Zlotogora J. Hum Genet. 1998 Apr;102(4):381-6. doi: 10.1007/s004390050708. Hum Genet. 1998. PMID: 9600231 Review.
Autosomal dominant inheritance with sex-limited infertility.
Daum H, Zlotogora J. Daum H, et al. Among authors: zlotogora j. Am J Med Genet A. 2023 Jun;191(6):1672-1674. doi: 10.1002/ajmg.a.63178. Epub 2023 Mar 9. Am J Med Genet A. 2023. PMID: 36891999 No abstract available.
The Israeli National Genetic Database.
Zlotogora J, van Baal S, Patrinos GP. Zlotogora J, et al. Isr Med Assoc J. 2009 Jun;11(6):373-5. Isr Med Assoc J. 2009. PMID: 19697591 Free article. Review.
International perspectives on the implementation of reproductive carrier screening.
Delatycki MB, Alkuraya F, Archibald A, Castellani C, Cornel M, Grody WW, Henneman L, Ioannides AS, Kirk E, Laing N, Lucassen A, Massie J, Schuurmans J, Thong MK, van Langen I, Zlotogora J. Delatycki MB, et al. Among authors: zlotogora j. Prenat Diagn. 2020 Feb;40(3):301-310. doi: 10.1002/pd.5611. Epub 2019 Nov 29. Prenat Diagn. 2020. PMID: 31774570 Review.
Medical genetics in Israel.
Zlotogora J, Chemke J. Zlotogora J, et al. Eur J Hum Genet. 1995;3(3):147-54. doi: 10.1159/000472290. Eur J Hum Genet. 1995. PMID: 7583040 Review.
Congenital cutis laxa.
Zlotogora J. Zlotogora J. Clin Genet. 1987 May;31(5):357. doi: 10.1111/j.1399-0004.1987.tb02822.x. Clin Genet. 1987. PMID: 3608223 No abstract available.
Biallelic variants in PAX3 cause Klein syndrome.
Salah S, Meiner V, Abumayaleh A, Asafra A, Al-Sharif T, Al-Fallah O, Hasasneh B, Zlotogora J. Salah S, et al. Among authors: zlotogora j. Clin Genet. 2022 Sep;102(3):223-227. doi: 10.1111/cge.14167. Epub 2022 Jun 5. Clin Genet. 2022. PMID: 35607853
210 results