Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

60 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Chromosome studies in IgA-deficient patients.
Taalman RD, Weemaes CM, Hustinx TW, Scheres JM, Clement JM, Stoelinga GB. Taalman RD, et al. Among authors: hustinx tw. Clin Genet. 1987 Aug;32(2):81-7. doi: 10.1111/j.1399-0004.1987.tb03330.x. Clin Genet. 1987. PMID: 3652494
Further delineation of the Nijmegen breakage syndrome.
Taalman RD, Hustinx TW, Weemaes CM, Seemanová E, Schmidt A, Passarge E, Scheres JM. Taalman RD, et al. Among authors: hustinx tw. Am J Med Genet. 1989 Mar;32(3):425-31. doi: 10.1002/ajmg.1320320332. Am J Med Genet. 1989. PMID: 2786340
Heritable fragility at 11q13 and 12q13.
Smeets DF, Scheres JM, Hustinx TW. Smeets DF, et al. Among authors: hustinx tw. Clin Genet. 1985 Aug;28(2):145-50. doi: 10.1111/j.1399-0004.1985.tb00374.x. Clin Genet. 1985. PMID: 4042396
Bloom's syndrome in two Dutch families.
Hustinx TW, Ter Haar BG, Scheres JM, Rutten FJ, Weemaes CM, Hoppe RL, Janssen AH. Hustinx TW, et al. Clin Genet. 1977 Aug;12(2):85-96. doi: 10.1111/j.1399-0004.1977.tb00907.x. Clin Genet. 1977. PMID: 891017
The most common fragile site in man is 3p14.
Smeets DF, Scheres JM, Hustinx TW. Smeets DF, et al. Among authors: hustinx tw. Hum Genet. 1986 Mar;72(3):215-20. doi: 10.1007/BF00291880. Hum Genet. 1986. PMID: 2937710
[Immunodeficiency and chromosome instability].
Weemaes CM, Bakkeren JA, Hustinx TW, van Munster PJ, Scheres JM. Weemaes CM, et al. Among authors: hustinx tw. Tijdschr Kindergeneeskd. 1988 Oct;56(5):209-12. Tijdschr Kindergeneeskd. 1988. PMID: 3206518 Dutch.
Trisomy for the short arm of chromosome No. 10.
Hustinx TW, Ter Haar BG, Scheres JM, Rutten FJ. Hustinx TW, et al. Clin Genet. 1974;6(5):408-15. doi: 10.1111/j.1399-0004.1974.tb02264.x. Clin Genet. 1974. PMID: 4434655 No abstract available.
The fragile site on chromosome 3.
Smeets DF, Scheres JM, Hustinx TW. Smeets DF, et al. Among authors: hustinx tw. Hum Genet. 1984;67(3):351. doi: 10.1007/BF00291369. Hum Genet. 1984. PMID: 6469246 No abstract available.
60 results