Guus Hamers - Concepedia

Author

Guus Hamers

Also Known As

G Hamers, G J Hamers, G. HAMERS, G. Hamers, G. J.H.Hamers, G.J.H. Hamers, Guus Hamers, Guus J. H. Hamers, Guus J.H. Hamers

Publications

531

Citations

H-Index

Concepts

All Affiliations

Maastricht University Maastricht University Medical Centre University of Groningen Erasmus University Rotterdam

About

Guus Hamers is an author at Maastricht University specializing in medicine, genetics, and cytogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	139
2	Natural Sciences	2	2	61
3	Public Health	2	2	30
4	Biomedical Engineering	1	1	46
5	Cell Biology	1	1	46

Guus Hamers

Publications

333

Citations

H-Index

Page 1

	Year	Citations
Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome H.-J. Lüdecke, M.J. Wagner, J. Nardmann, Human Molecular Genetics	1995	123
A simple and efficient method for microdissection and microFISH. J.J.M. Engelen, J.C.M. Albrechts, Guus Hamers, Journal of Medical Genetics Chromosome RegionEfficient MethodGeneticsDna AnalysisMolecular Biology	1998	46
Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patients Jacques C. Giltay, P.M.M. Kastrop, J.H.A.M. Tuerlings, Human Reproduction	1999	34
Translocation t(2;3)(p15–23;q26–27) in myeloid malignancies: report of 21 new cases, clinical, cytogenetic and molecular genetic features Marian Stevens‐Kroef, Bruce Poppe, Shama van Zelderen‐Bhola, Leukemia Hematological MalignancyMedicineHematologyImmunologyPathology	2004	32
Mosaic trisomy 11p in monozygotic twins with discordant clinical phenotypes D. Marcus‐Soekarman, Guus Hamers, S. Velzeboer, American Journal of Medical Genetics Part A CytogeneticsGeneticsGenetic EpidemiologyPathologyMolecular Genetics	2003	18
Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis Diane Van Opstal, Marjan Boter, Petra Noomen, Molecular Cytogenetics	2011	17
Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping H. J. DE LIEFDE MEIJER, Guus Hamers, Roselie Jongbloed, Human Genetics Down SyndromeChromatinDevelopmental BiologyCytogeneticsGenetic Disorder	1989	16
Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization J.J.M. Engelen, Wil J. G. Loots, Jozefa C.M. Albrechts, American Journal of Medical Genetics Developmental BiologyCytogeneticsNatural SciencesGeneticsMolecular Biological Method	1998	15
Prenatal diagnosis of trisomy 12 mosaicism: normal development of a 3 years old female child. J E A Staals, Ctrm Schrander-Stumpel, Guus Hamers, PubMed CytogeneticsGynecologyEmbryologyUterine AnomaliesAbnormal Development	2003	12
Marker chromosome identification by micro‐FISH J.J.M. Engelen, Wil J. G. Loots, Petra C. C. Motoh, Clinical Genetics	1996	10

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