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Author

Hustinx Tw

Observed name: T W Hustinx
OpenAlex ID: A5021037014
A familial syndrome of mental retardation in association with multiple congenital anomalies resembling the syndrome of Smith-Lemli-Opitz.
1967 · H Kenis, T W Hustinx · PubMed · 18
A case of partial 9p monosomy with some unusual clinical features.
1978 · F J Rutten, T W Hustinx, et al. · PubMed · 9
"Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case.
1965 · T W Hustinx, J C Wijffels · PubMed · 6
[Immunologic and cytogenetic aspects of ataxia telangiectasia].
1984 · C M Weemaes, R D Taalman, et al. · PubMed · 1
Results of a Cytogenetic Study on Children With Non-high Risk All at Diagnosis in Protocol Vi of the Dutch Childhood Leukemia Study-group - (dclsg)
1988 · Slater Rm, Hustinx Tw, et al. · University of Groningen research database (University of Groningen / Centre for Information Technology)
[Down's syndrome in the Netherlands].
1986 · T W Hustinx, J M Scheres, et al. · PubMed
[A Dutch chromosome abnormality in myelodysplasia?].
1985 · J M Scheres, T W Hustinx, et al. · PubMed
[The 47 XYY chromosome pattern in humans].
1970 · J G Rouwet, T W Hustinx · PubMed
[Chromosome aberrations in psychiatric patients].
1969 · T W Hustinx · PubMed
Works count: 9
Citation count: 34
H-index: 3
I10-index: 1
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