van Herwerden L - Search Results

1

Linkage analysis of bronchial hyperreactivity and atopy with chromosome 11q13.

Wong ZY, Tsonis D, van Herwerden L, Raven J, Forbes A, Abramson MJ, Walters EH, Harrap SB. Wong ZY, et al. Among authors: van herwerden l. Electrophoresis. 1997 Aug;18(9):1641-5. doi: 10.1002/elps.1150180928. Electrophoresis. 1997. PMID: 9378137

2

Linkage of high-affinity IgE receptor gene with bronchial hyperreactivity, even in absence of atopy.

van Herwerden L, Harrap SB, Wong ZY, Abramson MJ, Kutin JJ, Forbes AB, Raven J, Lanigan A, Walters EH. van Herwerden L, et al. Lancet. 1995 Nov 11;346(8985):1262-5. doi: 10.1016/s0140-6736(95)91863-9. Lancet. 1995. PMID: 7475718

3

Absence of genetic linkage of chromosome 5q31 with asthma and atopy in the general population.

Kamitani A, Wong ZY, Dickson P, van Herwerden L, Raven J, Forbes AB, Abramson MJ, Walters EH, Harrap SB. Kamitani A, et al. Among authors: van herwerden l. Thorax. 1997 Sep;52(9):816-7. doi: 10.1136/thx.52.9.816. Thorax. 1997. PMID: 9371215 Free PMC article.

4

The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p.

Brueton LA, van Herwerden L, Chotai KA, Winter RM. Brueton LA, et al. Among authors: van herwerden l. J Med Genet. 1992 Oct;29(10):681-5. doi: 10.1136/jmg.29.10.681. J Med Genet. 1992. PMID: 1433226 Free PMC article.

5

The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Brueton LA, Chotai KA, van Herwerden L, Schinzel A, Winter RM. Brueton LA, et al. Among authors: van herwerden l. J Med Genet. 1992 Sep;29(9):635-7. doi: 10.1136/jmg.29.9.635. J Med Genet. 1992. PMID: 1404293 Free PMC article.

6

Six cases of 7p deletion: clinical, cytogenetic, and molecular studies.

Chotai KA, Brueton LA, van Herwerden L, Garrett C, Hinkel GK, Schinzel A, Mueller RF, Speleman F, Winter RM. Chotai KA, et al. Among authors: van herwerden l. Am J Med Genet. 1994 Jul 1;51(3):270-6. doi: 10.1002/ajmg.1320510320. Am J Med Genet. 1994. PMID: 7521123 Review.

7

Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter.

Reardon W, van Herwerden L, Rose C, Jones B, Malcolm S, Winter RM. Reardon W, et al. Among authors: van herwerden l. J Med Genet. 1994 Mar;31(3):219-21. doi: 10.1136/jmg.31.3.219. J Med Genet. 1994. PMID: 8014970 Free PMC article.

8

Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5q.

van Herwerden L, Rose CS, Reardon W, Brueton LA, Weissenbach J, Malcolm S, Winter RM. van Herwerden L, et al. Am J Hum Genet. 1994 Apr;54(4):669-74. Am J Hum Genet. 1994. PMID: 8128964 Free PMC article.

9

Risk of strut fracture of Björk-Shiley valves.

van der Graaf Y, de Waard F, van Herwerden LA, Defauw J. van der Graaf Y, et al. Among authors: van herwerden la. Lancet. 1992 Feb 1;339(8788):257-61. doi: 10.1016/0140-6736(92)91328-6. Lancet. 1992. PMID: 1346279

10

Single-leg strut fractures in explanted Björk-Shiley valves.

de Mol BA, Kallewaard M, McLellan RB, van Herwerden LA, Defauw JJ, van der Graaf Y. de Mol BA, et al. Among authors: van der graaf y, van herwerden la. Lancet. 1994 Jan 1;343(8888):9-12. doi: 10.1016/s0140-6736(94)90874-5. Lancet. 1994. PMID: 7905086

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