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Results by year

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

Year Number of Results
1970 1
1973 4
1974 1
1975 2
1976 3
1977 1
1978 5
1979 3
1980 4
1981 2
1982 2
1983 5
1984 7
1985 7
1986 5
1987 3
1988 6
1989 4
1990 10
1991 8
1992 7
1993 6
1994 9
1995 11
1996 9
1997 10
1998 14
1999 9
2000 7
2001 7
2002 6
2003 3
2004 6
2005 3
2006 8
2007 3
2008 2
2012 2
2024 0

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204 results

Results by year

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Page 1
Glycogenosis type II (acid maltase deficiency).
Reuser AJ, Kroos MA, Hermans MM, Bijvoet AG, Verbeet MP, Van Diggelen OP, Kleijer WJ, Van der Ploeg AT. Reuser AJ, et al. Among authors: kleijer wj. Muscle Nerve Suppl. 1995;3:S61-9. doi: 10.1002/mus.880181414. Muscle Nerve Suppl. 1995. PMID: 7603530 Free article. Review.
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency.
Van Kuilenburg AB, Vreken P, Abeling NG, Bakker HD, Meinsma R, Van Lenthe H, De Abreu RA, Smeitink JA, Kayserili H, Apak MY, Christensen E, Holopainen I, Pulkki K, Riva D, Botteon G, Holme E, Tulinius M, Kleijer WJ, Beemer FA, Duran M, Niezen-Koning KE, Smit GP, Jakobs C, Smit LM, Van Gennip AH, et al. Van Kuilenburg AB, et al. Among authors: kleijer wj. Hum Genet. 1999 Jan;104(1):1-9. doi: 10.1007/pl00008711. Hum Genet. 1999. PMID: 10071185 Review.
Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome.
Chrzanowska KH, Kleijer WJ, Krajewska-Walasek M, Białecka M, Gutkowska A, Goryluk-Kozakiewicz B, Michałkiewicz J, Stachowski J, Gregorek H, Lysón-Wojciechowska G, et al. Chrzanowska KH, et al. Among authors: kleijer wj. Am J Med Genet. 1995 Jul 3;57(3):462-71. doi: 10.1002/ajmg.1320570321. Am J Med Genet. 1995. PMID: 7545870 Review.
[Menkes syndrome].
Zeman J, Houst'ková H, Hyánek J, Rubín A, Kleijer WJ, Komárek V, Jirásek A, Mandys V. Zeman J, et al. Among authors: kleijer wj. Cesk Pediatr. 1987 Feb;42(2):102-3. Cesk Pediatr. 1987. PMID: 3568170 Czech. No abstract available.
Prenatal diagnosis and genetic counseling of cystic fibrosis.
Niermeijer MF, Halley DJ, Kleijer WJ, Neijens HJ, Sinaasappel M. Niermeijer MF, et al. Among authors: kleijer wj. Acta Paediatr Scand Suppl. 1989;363:20-4. doi: 10.1111/apa.1989.78.s363.20. Acta Paediatr Scand Suppl. 1989. PMID: 2701920 Review.
Atypical clinical presentation of ataxia telangiectasia.
Willems PJ, Van Roy BC, Kleijer WJ, Van der Kraan M, Martin JJ. Willems PJ, et al. Among authors: kleijer wj. Am J Med Genet. 1993 Mar 15;45(6):777-82. doi: 10.1002/ajmg.1320450624. Am J Med Genet. 1993. PMID: 8456862 Review.
Fatal neonatal malonic aciduria.
Buyukgebiz B, Jakobs C, Scholte HR, Huijmans JG, Kleijer WJ. Buyukgebiz B, et al. Among authors: kleijer wj. J Inherit Metab Dis. 1998 Feb;21(1):76-7. doi: 10.1023/a:1005371616609. J Inherit Metab Dis. 1998. PMID: 9501274 No abstract available.
Molecular basis of androgen insensitivity.
Brüggenwirth HT, Boehmer AL, Verleun-Mooijman MC, Hoogenboezem T, Kleijer WJ, Otten BJ, Trapman J, Brinkmann AO. Brüggenwirth HT, et al. Among authors: kleijer wj. J Steroid Biochem Mol Biol. 1996 Aug;58(5-6):569-75. doi: 10.1016/0960-0760(96)00095-7. J Steroid Biochem Mol Biol. 1996. PMID: 8918984
Prenatal diagnosis of genetic disorders.
Niermeijer MF, Sachs ES, Jahodova M, Tichelaar-Klepper C, Kleijer WJ, Galjaard H. Niermeijer MF, et al. Among authors: kleijer wj. J Med Genet. 1976 Jun;13(3):182-94. doi: 10.1136/jmg.13.3.182. J Med Genet. 1976. PMID: 58990 Free PMC article.
204 results