Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype
Bijlsma, E K, Aalfs, C M, Sluijter, S, Luttikhuis, M E M Oude, Trembath, R C, Hoovers, J M N, Hennekam, R C M
Published in Journal of medical genetics (01.08.1999)
Published in Journal of medical genetics (01.08.1999)
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Four DAZ Genes in Two Clusters Found in the AZFc Region of the Human Y Chromosome
Saxena, Richa, de Vries, Jan W.A., Repping, Sjoerd, Alagappan, Raaji K., Skaletsky, Helen, Brown, Laura G., Ma, Peter, Chen, Ellson, Hoovers, Jan M.N., Page, David C.
Published in Genomics (San Diego, Calif.) (01.08.2000)
Published in Genomics (San Diego, Calif.) (01.08.2000)
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Progression from colorectal adenoma to carcinoma is associated with non-random chromosomal gains as detected by comparative genomic hybridisation
Meijer, G A, Hermsen, M A, Baak, J P, van Diest, P J, Meuwissen, S G, Beliën, J A, Hoovers, J M, Joenje, H, Snijders, P J, Walboomers, J M
Published in Journal of clinical pathology (01.12.1998)
Published in Journal of clinical pathology (01.12.1998)
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FISH mapping of three ammonia metabolism genes (Glul, Cps1, Glud1) in rat, and the chromosomal localization of GLUL in human and Cps1 in mouse
Helou, K, Das, A T, Lamers, W H, Hoovers, J M, Szpirer, C, Szpirer, J, Klinga-Levan, K, Levan, G
Published in Mammalian genome (01.05.1997)
Published in Mammalian genome (01.05.1997)
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Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization
Schuring-Blom, G H, Keijzer, M, Jakobs, M E, Van den Brande, D M, Visser, H M, Wiegant, J, Hoovers, J M, Leschot, N J
Published in Prenatal diagnosis (01.08.1993)
Published in Prenatal diagnosis (01.08.1993)
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High-resolution in situ hybridization using DNA halo preparations
Wiegant, J, Kalle, W, Mullenders, L, Brookes, S, Hoovers, J M, Dauwerse, J G, van Ommen, G J, Raap, A K
Published in Human molecular genetics (01.11.1992)
Published in Human molecular genetics (01.11.1992)
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Multiple Genetic Loci within 11p15 Defined by Beckwith-Wiedemann Syndrome Rearrangement Breakpoints and Subchromosomal Transferable Fragments
Hoovers, J M, Kalikin, L M, Johnson, L A, Alders, M, Redeker, B, Law, D J, Bliek, J, Steenman, M, Benedict, M, Wiegant, J, Lengauer, C, Taillon-Miller, P, Schlessinger, D, Edwards, M C, Elledge, S J, Ivens, A, Westerveld, A, Little, P, Mannens, M, Feinberg, A P
Published in Proceedings of the National Academy of Sciences - PNAS (19.12.1995)
Published in Proceedings of the National Academy of Sciences - PNAS (19.12.1995)
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Journal Article
Partial trisomy and monosomy 8p due to inversion duplication
Engelen, J J, de Die-Smulders, C E, Fryns, J P, Hoovers, J M, Albrechts, J C, Loots, W J, Jacobs, M E, Hamers, A J
Published in Clinical genetics (01.04.1994)
Published in Clinical genetics (01.04.1994)
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Celsr1, a Neural-Specific Gene Encoding an Unusual Seven-Pass Transmembrane Receptor, Maps to Mouse Chromosome 15 and Human Chromosome 22qter
Hadjantonakis, Anna-Katerina, Sheward, W.John, Harmar, Anthony J., de Galan, Louis, Hoovers, Jan M.N., Little, Peter F.R.
Published in Genomics (San Diego, Calif.) (01.10.1997)
Published in Genomics (San Diego, Calif.) (01.10.1997)
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An aetiological study of 25 mentally retarded adults with autism
van Karnebeek, C D M, van Gelderen, I, Nijhof, G J, Abeling, N G, Vreken, P, Redeker, E J, van Eeghen, A M, Hoovers, J M N, Hennekam, R C M
Published in Journal of medical genetics (01.03.2002)
Published in Journal of medical genetics (01.03.2002)
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Multiple and sensitive fluorescence in situ hybridization with rhodamine-, fluorescein-, and coumarin-labeled DNAs
Wiegant, J, Wiesmeijer, C C, Hoovers, J M, Schuuring, E, d'Azzo, A, Vrolijk, J, Tanke, H J, Raap, A K
Published in Cytogenetics and cell genetics (1993)
Published in Cytogenetics and cell genetics (1993)
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First-trimester non-invasive prenatal diagnosis of triploidy
de Graaf, Irene M., van Bezouw, Saskia M. C. A., Jakobs, Marja E., Leschot, Nico J., Zondervan, Hans A., Bilardo, Caterina M., Hoovers, Jan M. N.
Published in Prenatal diagnosis (01.02.1999)
Published in Prenatal diagnosis (01.02.1999)
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Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: dose effect of the PAX6 gene product?
Aalfs, C M, Fantes, J A, Wenniger-Prick, L J, Sluijter, S, Hennekam, R C, van Heyningen, V, Hoovers, J M
Published in American journal of medical genetics (19.12.1997)
Published in American journal of medical genetics (19.12.1997)
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Further delineation of the partial proximal trisomy 10q syndrome
Aalfs, C M, Hoovers, J M, Nieste-Otter, M A, Mannens, M M, Hennekam, R C, Leschot, N J
Published in Journal of medical genetics (01.12.1995)
Published in Journal of medical genetics (01.12.1995)
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High-Resolution Chromosomal Localization of the Human Calcitonin/CGRP/IAPP Gene Family Members
Hoovers, J.M.N., Redeker, E., Speleman, F., Höppener, J.W.M., Bhola, S., Bliek, J., van Roy, N., Leschot, N.J., Westerveld, A., Mannens, M.
Published in Genomics (San Diego, Calif.) (01.03.1993)
Published in Genomics (San Diego, Calif.) (01.03.1993)
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