Výsledky vyhledávání - "Vd Smagt, J. J."

National registry for patients and families with a familial heart disease

Autor: Pinto, Y. M., Wilde, A. A. M., Hermans-Van Ast, J. F., Langen, I. M., Tintelen, J. P., Atsma, D. E., Arens, Y. M., Marcelis, C. L., Folkert ten Cate, Vd Smagt, J. J., Houweling, A. C.

Publikováno v: Netherlands heart journal, 17(2). Bohn Stafleu van Loghum
University of Groningen
Netherlands Heart Journal, 17(2). Bohn, Stafleu, Van Loghum
Scopus-Elsevier

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::538416533888826eab5a9c57586233dd
https://pure.amc.nl/en/publications/national-registry-for-patients-and-families-with-a-familial-heart-disease(ac2f0e82-0be5-46d5-9bcf-fa6aa77a3620).html

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National registry for patients and families with a familial heart disease Project leaders

Autor: Pinto, Y. M., Wilde, A. A. M., Hermans-Van Ast, J. F., Wilde, A. A., Langen, I. M., Tintelen, J. P., Atsma, D. E., Arens, Y. M., Marcelis, C. L., Folkert ten Cate, Vd Smagt, J. J., Houweling, A. C.

Publikováno v: University of Groningen
Scopus-Elsevier
Pinto, Y M, Wilde, A A M, Hermans-van Ast, J F, Wilde, A A, Van Langen, I M, Van Tintelen, J P, Atsma, D E, Arens, Y M, Marcelis, C L, Ten Cate, F J, Vd Smagt, J J & Houweling, A C 2009, ' National registry for patients and families with a familial heart disease Project leaders ', Netherlands Heart Journal, vol. 17, no. 1, pp. 40 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::525809b095465fed447ff8d180999b4e
https://research.rug.nl/en/publications/b53b0685-3e60-430c-ab03-a900901e7bcc

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A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome)

Autor: Brooks, A. S., Breuning, M. H., Osinga, J., Vd Smagt, J. J., Catsman, C. E., Buys, C. H. C. M., Meijers, C., Robert Hofstra

Publikováno v: Scopus-Elsevier
JOURNAL OF MEDICAL GENETICS, 36(6), 485-489. BMJ PUBLISHING GROUP
Journal of Medical Genetics, 36, 485-489. BMJ Publishing Group

Hirschsprung disease, mental retardation, microcephaly, and specific craniofacial dysmorphism were observed in three children from a large, consanguineous, Moroccan family. A fourth child showed similar clinical features, with the exception of Hirsch

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f741356c287cf6aea41ebdbb83e20155
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033036664&partnerID=MN8TOARS

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