المؤلفون: van Andel, H^{Aff1, Aff2}, Kocemba, K A^{Aff1, Aff2, Aff3}, de Haan-Kramer, A^{Aff1, Aff2}, Mellink, C H, Piwowar, M, Broijl, A, van Duin, M, Sonneveld, P, Maurice, M M, Kersten, M J^{Aff2, Aff8}, Spaargaren, M^{Aff1, Aff2}, Pals, S T^{Aff1, Aff2, IDonc2016368_cor12}

المصدر: Oncogene. 36(15):2105-2115

المؤلفون: Mous, R, Jaspers, A, Luijks, D M P, Mellink, C H M, van Oers, M H J, Kater, A P, Eldering, E^{Aff3, IDleu200971_cor7}

المصدر: Leukemia. 23(7):1352-1355

المؤلفون: Gunn, S R^{Aff1, Aff2}, Hibbard, M K, Ismail, S H, Lowery-Nordberg, M, Mellink, C H M, Bahler, D W, Abruzzo, L V, Enriquez, E L, Gorre, M E, Mohammed, M S, Robetorye, R S^{Aff2, IDleu2008393_cor11}

المصدر: Leukemia. 23(5):1011-1017

المؤلفون: Archibald, A. L., Couperwhite, S., Mellink, C. H. M., Lahbib-Mansais, Y., Gellin, J.

المصدر: Animal Genetics; Apr1996, Vol. 27 Issue 2, p85-90, 6p

المؤلفون: MELLINK, C. H. M., BOSMA, A. A., HAAN, N. A., MACDONALD, A. A.

المصدر: Animal Genetics; Jun1992, Vol. 23 Issue 3, p231-239, 9p

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المؤلفون: Mellink CH; Department of Clinical Genetics, Academic Medical Center, 1100 DE Amsterdam, The Netherlands. c.h.mellink@amc.uva.nl, Alders M, van der Lelie H, Hennekam RH, Kuijpers TW

المصدر: Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2004 Oct 15; Vol. 154 (2), pp. 144-9.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Elsevier/North-Holland Country of Publication: United States NLM ID: 7909240 Publication Model: Print Cited Medium: Print ISSN: 0165-4608 (Print) Linking ISSN: 01654608 NLM ISO Abbreviation: Cancer Genet Cytogenet Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 7* , Isochromosomes*, Anemia, Aplastic/*genetics , Exocrine Pancreatic Insufficiency/*genetics , Musculoskeletal Abnormalities/*genetics , Proteins/*genetics, Adult ; Base Sequence ; Disease Susceptibility ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Mutation ; Myelodysplastic Syndromes/etiology ; Syndrome

عنوان ترانسليتريتد: Fluorescentie-in-situhybridisatie bij het onderzoek naar chromosomale afwijkingen.

المؤلفون: Hoovers JM; Academisch Medisch Centrum, afd. Klinische Genetica, Amsterdam., Mellink CH, Leschot NJ

المصدر: Nederlands tijdschrift voor geneeskunde [Ned Tijdschr Geneeskd] 1999 Nov 06; Vol. 143 (45), pp. 2265-8.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Vereniging NTvG Country of Publication: Netherlands NLM ID: 0400770 Publication Model: Print Cited Medium: Print ISSN: 0028-2162 (Print) Linking ISSN: 00282162 NLM ISO Abbreviation: Ned Tijdschr Geneeskd Subsets: MEDLINE

مواضيع طبية MeSH: DNA Mutational Analysis*, Chromosome Aberrations/*diagnosis , Chromosome Aberrations/*genetics , In Situ Hybridization, Fluorescence/*statistics & numerical data, Chromosome Deletion ; Chromosome Disorders ; Cytogenetic Analysis ; DNA Probes ; Humans ; Microsatellite Repeats ; Syndrome ; Translocation, Genetic ; Trisomy/diagnosis ; Trisomy/genetics

المؤلفون: Zijlstra C; Department of Cell Biology and Histology, Faculty of Veterinary Medicine, Utrecht University, The Netherlands. fumocelb@pobox.ruu.nl, Mellink CH, de Haan NA, Bosma AA

المصدر: Cytogenetics and cell genetics [Cytogenet Cell Genet] 1997; Vol. 77 (3-4), pp. 273-7.

نوع المنشور: Comparative Study; Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0367735 Publication Model: Print Cited Medium: Print ISSN: 0301-0171 (Print) Linking ISSN: 03010171 NLM ISO Abbreviation: Cytogenet Cell Genet Subsets: MEDLINE

مواضيع طبية MeSH: Artiodactyla/*genetics , DNA, Ribosomal/*genetics, Animals ; Artiodactyla/classification ; Chromosome Banding ; Chromosome Mapping ; DNA Probes ; In Situ Hybridization, Fluorescence ; RNA, Ribosomal/genetics ; RNA, Ribosomal, 18S/genetics ; RNA, Ribosomal, 5.8S/genetics ; RNA, Ribosomal, 5S/genetics ; Species Specificity