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

Year Number of Results
1976 1
1981 1
1982 1
1983 3
1984 3
1985 3
1986 1
1988 2
1989 1
1990 2
1992 4
1994 2
1995 3
1996 7
1997 2
1998 3
1999 1
2000 5
2001 1
2002 2
2003 1
2004 1
2005 6
2006 3
2007 4
2009 1
2011 2
2012 4
2016 1
2017 1
2024 0

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68 results

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Page 1
[Diagnosis of vitamin B12 deficiency revised].
Wiersinga WJ, de Rooij SE, Huijmans JG, Fischer C, Hoekstra JB. Wiersinga WJ, et al. Among authors: huijmans jg. Ned Tijdschr Geneeskd. 2005 Dec 10;149(50):2789-94. Ned Tijdschr Geneeskd. 2005. PMID: 16385831 Review. Dutch.
Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib).
Schollen E, Dorland L, de Koning TJ, Van Diggelen OP, Huijmans JG, Marquardt T, Babovic-Vuksanovic D, Patterson M, Imtiaz F, Winchester B, Adamowicz M, Pronicka E, Freeze H, Matthijs G. Schollen E, et al. Among authors: huijmans jg. Hum Mutat. 2000 Sep;16(3):247-52. doi: 10.1002/1098-1004(200009)16:3<247::AID-HUMU7>3.0.CO;2-A. Hum Mutat. 2000. PMID: 10980531 Review.
The live-birth prevalence of mucopolysaccharidoses in Estonia.
Krabbi K, Joost K, Zordania R, Talvik I, Rein R, Huijmans JG, Verheijen FV, Õunap K. Krabbi K, et al. Among authors: huijmans jg. Genet Test Mol Biomarkers. 2012 Aug;16(8):846-9. doi: 10.1089/gtmb.2011.0307. Epub 2012 Apr 5. Genet Test Mol Biomarkers. 2012. PMID: 22480138 Free PMC article.
Prenatal diagnosis of the urea cycle diseases: a survey of the European cases.
Kamoun P, Fensom AH, Shin YS, Bakker E, Colombo JP, Munnich A, Bird S, Canini S, Huijmans JG, Chadefaux-Vekemans B, et al. Kamoun P, et al. Among authors: huijmans jg. Am J Med Genet. 1995 Jan 16;55(2):247-50. doi: 10.1002/ajmg.1320550220. Am J Med Genet. 1995. PMID: 7717428 Review.
Fatal neonatal malonic aciduria.
Buyukgebiz B, Jakobs C, Scholte HR, Huijmans JG, Kleijer WJ. Buyukgebiz B, et al. Among authors: huijmans jg. 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.
First-trimester diagnosis of Morquio disease type A.
Kleijer WJ, Geilen GC, Garritsen V, Huijmans JG, Los FJ, Voznyi YV, van Diggelen OP. Kleijer WJ, et al. Among authors: huijmans jg. Prenat Diagn. 2000 Mar;20(3):183-5. Prenat Diagn. 2000. PMID: 10719317
Black discolouration of urine in two young sisters.
Martens T, van Gammeren AJ, Huijmans JG, de Man SA. Martens T, et al. Among authors: huijmans jg. J Paediatr Child Health. 2016 Jun;52(6):680-1. doi: 10.1111/jpc.13022. J Paediatr Child Health. 2016. PMID: 27333853 No abstract available.
68 results