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

Year Number of Results
1986 1
1987 2
1989 4
1990 2
1991 1
1992 3
1997 1
1999 1
2000 2
2024 0

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Page 1
Oculoauriculovertebral spectrum and cerebral anomalies.
Schrander-Stumpel CT, de Die-Smulders CE, Hennekam RC, Fryns JP, Bouckaert PX, Brouwer OF, da Costa JJ, Lommen EJ, Maaswinkel-Mooy PD. Schrander-Stumpel CT, et al. Among authors: maaswinkel mooy pd. J Med Genet. 1992 May;29(5):326-31. doi: 10.1136/jmg.29.5.326. J Med Genet. 1992. PMID: 1583660 Free PMC article. Review.
[Metabolic acidosis in children: the usefulness of 'anion gap'].
Kist-van Holthe tot Echten JE, Maaswinkel-Mooy PD, Berger HM, van der Heijden AJ. Kist-van Holthe tot Echten JE, et al. Among authors: maaswinkel mooy pd. Ned Tijdschr Geneeskd. 1999 Mar 27;143(13):649-51. Ned Tijdschr Geneeskd. 1999. PMID: 10321293 Review. Dutch.
Familial vascular retinopathy. A preliminary report.
Storimans CW, Oosterhuis JA, van Schooneveld MJ, Bos PJ, Maaswinkel-Mooy PD. Storimans CW, et al. Among authors: maaswinkel mooy pd. Doc Ophthalmol. 1990 Oct;75(3-4):259-61. doi: 10.1007/BF00164839. Doc Ophthalmol. 1990. PMID: 2090400
Hepatocellular carcinoma in glycogen storage disease type IV.
de Moor RA, Schweizer JJ, van Hoek B, Wasser M, Vink R, Maaswinkel-Mooy PD. de Moor RA, et al. Among authors: maaswinkel mooy pd. Arch Dis Child. 2000 Jun;82(6):479-80. doi: 10.1136/adc.82.6.479. Arch Dis Child. 2000. PMID: 10833181 Free PMC article.
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations.
Petrij F, Dauwerse HG, Blough RI, Giles RH, van der Smagt JJ, Wallerstein R, Maaswinkel-Mooy PD, van Karnebeek CD, van Ommen GJ, van Haeringen A, Rubinstein JH, Saal HM, Hennekam RC, Peters DJ, Breuning MH. Petrij F, et al. Among authors: maaswinkel mooy pd. J Med Genet. 2000 Mar;37(3):168-76. doi: 10.1136/jmg.37.3.168. J Med Genet. 2000. PMID: 10699051 Free PMC article.
17 results