van Oost BA - Search Results

1

X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism.

Brunner HG, Nelen MR, van Zandvoort P, Abeling NG, van Gennip AH, Wolters EC, Kuiper MA, Ropers HH, van Oost BA. Brunner HG, et al. Among authors: van gennip ah, van oost ba, van zandvoort p. Am J Hum Genet. 1993 Jun;52(6):1032-9. Am J Hum Genet. 1993. PMID: 8503438 Free PMC article.

2

Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation.

Traupe H, Müller D, Atherton D, Kalter DC, Cremers FP, van Oost BA, Ropers HH. Traupe H, et al. Among authors: van oost ba. Hum Genet. 1992 Aug;89(6):659-65. doi: 10.1007/BF00221958. Hum Genet. 1992. PMID: 1355069

3

Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2.

Oosterwijk JC, Nelen M, van Zandvoort PM, van Osch LD, Oranje AP, Wittebol-Post D, van Oost BA. Oosterwijk JC, et al. Among authors: van oost ba, van zandvoort pm, van osch ld. Am J Hum Genet. 1992 Apr;50(4):801-7. Am J Hum Genet. 1992. PMID: 1550124 Free PMC article.

4

Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis.

van Oost BA, van Zandvoort PM, Tünte W, Brunner HG, Hoogeboom AJ, Maaswinkel-Mooy PD, Bakkeren J, Hamel B, Ropers HH. van Oost BA, et al. Among authors: van zandvoort pm. Hum Genet. 1991 Feb;86(4):404-7. doi: 10.1007/BF00201845. Hum Genet. 1991. PMID: 1671851

5

An NcoI restriction fragment length polymorphism at the human steroid sulphatase gene locus.

van Zandvoort PM, van Bennekom CA, Ropers HH, van Oost BA. van Zandvoort PM, et al. Among authors: van oost ba, van bennekom ca. Hum Genet. 1990 Apr;84(5):489-90. doi: 10.1007/BF00195828. Hum Genet. 1990. PMID: 1969847

6

Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).

Brunner HG, Korneluk RG, Coerwinkel-Driessen M, MacKenzie A, Smeets H, Lambermon HM, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: van oost ba. Hum Genet. 1989 Mar;81(4):308-10. doi: 10.1007/BF00283680. Hum Genet. 1989. PMID: 2703233

7

Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome.

Knoers N, van der Heyden H, van Oost BA, Ropers HH, Monnens L, Willems J. Knoers N, et al. Among authors: van oost ba, van der heyden h. Hum Genet. 1988 Sep;80(1):31-8. doi: 10.1007/BF00451451. Hum Genet. 1988. PMID: 2843456

8

The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.

Wijker M, Ligtenberg MJ, Schoute F, Defesche JC, Pals G, Bolhuis PA, Ropers HH, Hulsebos TJ, Menko FH, van Oost BA, et al. Wijker M, et al. Among authors: van oost ba. Am J Hum Genet. 1995 May;56(5):1096-100. Am J Hum Genet. 1995. PMID: 7726164 Free PMC article.

9

Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A.

Brunner HG, Nelen M, Breakefield XO, Ropers HH, van Oost BA. Brunner HG, et al. Among authors: van oost ba. Science. 1993 Oct 22;262(5133):578-80. doi: 10.1126/science.8211186. Science. 1993. PMID: 8211186

10

X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorder.

de Vries DD, de Wijs IJ, Wolff G, Ketelsen UP, Ropers HH, van Oost BA. de Vries DD, et al. Among authors: van oost ba. Hum Genet. 1993 Mar;91(1):51-4. doi: 10.1007/BF00230222. Hum Genet. 1993. PMID: 8454287

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