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Hypercalcemia and diffuse osteolytic lesions in the acute phase of chronic myelogenous leukemia. A possible relation between lymphoid transformation and hypercalcemia.
Published in:
1983
By:
- Tricot, G.;
- Boogaerts, M. A.;
- Orshoven, A. Broeckaert-Van;
- Criel, A.;
- Van Hoof, A.;
- Van Berghe, H. Den;
- Broeckaert-Van Orshoven, A;
- Van den Berghe, H
Publication type:
journal article
A laboratory rainfall simulator study for determining the nutrient erodibility of an oxisol.
Published in:
Journal of the Science of Food & Agriculture, 1979, v. 30, n. 5, p. 532, doi. 10.1002/jsfa.2740300515
By:
- Van Berghe, C. H. Den;
- De Boodt, Marcelle F.
Publication type:
Article
Cytogenetic Findings in Moderate and Severe Mental Retardation A Study of an Institutionalized Population of 1991 Patients.
Published in:
Acta Paediatrica, 1984, v. 73, n. s313, p. 3, doi. 10.1111/j.1651-2227.1984.tb10001.x
By:
- FRYNS, J. P.;
- KLECZKOWSKA, A.;
- KUBIEŃ, E.;
- BERGHE, H. VAN DEN
Publication type:
Article
ZYGOSITY DETERMINATON AT BIRTH: A PLEA TO THE OBSTETRICIAN.
Published in:
Journal of Perinatal Medicine, 1991, v. 19, p. 234
By:
- DEROM, R.;
- VLIETINCK, R. F.;
- DEROM, C.;
- KEITH, L. G.;
- VAN DEN BERGHE, H.
Publication type:
Article
TWIN PREGNANCIES AFTER MEDICALLY ASSISTED REPRODUCTION: epidemiology, comparative perinatal morbidity and mortality.
Published in:
Journal of Perinatal Medicine, 1991, v. 19, p. 229
By:
- DEROM, R.;
- DEROM, C.;
- VLIETINCK, R.;
- VAN MAELE, G.;
- VAN DEN BERGHE, H.
Publication type:
Article
A new characteristic karyotypic anomaly in lymphoproliferative disorders.
Published in:
1979
By:
- Van Den Berghe, H.;
- Parloir, C.;
- David, G.;
- Michaux, J. L.;
- Sokal, G.
Publication type:
journal article
Chromosomes and causation of human cancer and leukemia. XXXI. Dq- deletions and their significance in proliferative diorders.
Published in:
Cancer (0008543X), 1979, v. 43, n. 4, p. 1350, doi. 10.1002/1097-0142(197904)43:4<1350::AID-CNCR2820430425>3.0.CO;2-#
By:
- Kohno, Sei-Ichi;
- Van Den Berghe, H.;
- Sandberg, Avery A.
Publication type:
Article
Chromosome abnormalities in acute promyelocytic leukemia (APL).
Published in:
Cancer (0008543X), 1979, v. 43, n. 2, p. 558, doi. 10.1002/1097-0142(197902)43:2<558::AID-CNCR2820430223>3.0.CO;2-6
By:
- Van Den Berghe, H.;
- Louwagie, A.;
- Van Orshoven, A. Broeckaert;
- David, G.;
- Verwilghen, R.;
- Michaux, J. L.;
- Sokal, G.
Publication type:
Article
Myofibroblastoma of the breast: genetic link with spindle cell lipoma.
Published in:
Journal of Pathology, 2000, v. 191, n. 3, p. 282, doi. 10.1002/1096-9896(2000)9999:9999<::AID-PATH635>3.0.CO;2-R
By:
- Pauwels, P.;
- Sciot, R.;
- Croiset, F.;
- Rutten, H.;
- Van den Berghe, H.;
- Dal Cin, P.
Publication type:
Article
Fluorescence in situ hybridization for the detection and monitoring of the Ph-positive clone in chronic myelogenous leukemia: comparison with metaphase banding analysis.
Published in:
1998
By:
- Cuneo, A.;
- Bigon, R.;
- Emmanuel, B.;
- Smit, E.;
- Rigolin, G.M.;
- Roberti, M.G.;
- Bardi, A.;
- Piva, N.;
- Scapoli, G.;
- Castoldi, G.;
- van Den Berghe, H.;
- Hagemeijer, A.;
- Bigoni, R
Publication type:
journal article
Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization.
Published in:
1997
By:
- Dierlamm, J;
- Rosenberg, C;
- Stul, M;
- Pittaluga, S;
- Wlodarska, I;
- Michaux, L;
- Dehaen, M;
- Verhoef, G;
- Thomas, J;
- de Kelver, W;
- Bakker-Schut, T;
- Cassiman, J J;
- Raap, A K;
- De Wolf-Peeters, C;
- Van den Berghe, H;
- Hagemeijer, A
Publication type:
journal article
Immature teratoma of the pineal gland with isochromosome 12p.
Published in:
Acta Neuropathologica, 1997, v. 95, n. 1, p. 107, doi. 10.1007/s004010050772
By:
- Cin, P. Dal;
- Tos, A. P. Dei;
- Qi, H.;
- Giannini, C.;
- Furlanetto, Alberto;
- Longatti, Pier Luigi;
- Marynen, Peter;
- den Berghe, H. Van
Publication type:
Article
Ciliogenesis in cultured human nasal epithelium.
Published in:
1990
By:
- Jorissen, Mark;
- van der Schueren, Bernadette;
- van den Berghe, Herman;
- Cassiman, Jean-Jacques;
- Jorissen, M;
- Van der Schueren, B;
- Van den Berghe, H;
- Cassiman, J J
Publication type:
journal article
No chromosome arm unturned: in memory of Roland Berger 1934-2012.
Published in:
Leukemia (08876924), 2014, v. 28, n. 2, p. 464, doi. 10.1038/leu.2013.340
By:
- Harrison, C J;
- Rowley, J D;
- Van den Berghe, H;
- Bernheim, A;
- Martineau, M;
- Gautier, M;
- Le Coniat-Busson, M;
- Romana, S;
- Dastugue, N;
- Hagemeijer, A;
- Jonveaux, P;
- Nguyen-Khac, F;
- Bernard, O A
Publication type:
Article
Elliptocytosis and Schistocytosis in Myelodysplasia: Report of Two Cases.
Published in:
Acta Haematologica, 1986, v. 75, n. 3, p. 174, doi. 10.1159/000206114
By:
- Rummens, J.L.;
- Verfaillie, C.;
- Criel, A.;
- Hidajat, M.;
- Vanhoof, A.;
- Van den Berghe, H.;
- Louwagie, A.
Publication type:
Article
t (9; 11) (p21; q22) Translocation in Acute Monoblastic Leukemia M5A-FAB.
Published in:
Acta Haematologica, 1984, v. 72, n. 3, p. 201, doi. 10.1159/000206387
By:
- Mecucci, C.;
- Tricot, G.;
- Van den Berghe, H.
Publication type:
Article
Hidden paracentric inversions of chromosome arm 12q affecting the HMGIC gene.
Published in:
Genes, Chromosomes & Cancer, 1997, v. 18, n. 4, p. 322, doi. 10.1002/(SICI)1098-2264(199704)18:4<322::AID-GCC13>3.0.CO;2-I
By:
- Wanschura, S.;
- Cin, P. Dal;
- Kazmierczak, B.;
- Bartnitzke, S.;
- Van den Berghe, H.;
- Bullerdiek, J.
Publication type:
Article
Genetic abnormalities in marginal zone B-cell lymphoma.
Published in:
2000
By:
- Dierlamm, Judith;
- Wlodarska, Iwona;
- Michaux, Lucienne;
- Stefanova, Margarita;
- Hinz, Kristina;
- Van den Berghe, Herman;
- Hagemeijer, Anne;
- Kurt Hossfeld, Dieter;
- Dierlamm, J;
- Wlodarska, I;
- Michaux, L;
- Stefanova, M;
- Hinz, K;
- Van Den Berghe, H;
- Hagemeijer, A;
- Hossfeld, D K
Publication type:
journal article
Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP Study Group.
Published in:
Histopathology, 2000, v. 37, n. 3, p. 212, doi. 10.1046/j.1365-2559.2000.00947.x
By:
- Vanni, R;
- Fletcher, C D M;
- Sciot, R;
- Dal Cin, P;
- De Wever, I;
- Mandahl, N;
- Mertens, F;
- Mitelman, F;
- Rosai, J;
- Rydholm, A;
- Tallini, G;
- van den Berghe, H;
- Willén, H
Publication type:
Article
Lesions of 13q may occur independently of deletion of 16q in spindle cell/pleomorphic lipomas.
Published in:
Histopathology, 1997, v. 31, n. 3, p. 222, doi. 10.1046/j.1365-2559.1997.2450851.x
By:
- DAL CIN, P.;
- SCIOT, R.;
- POLITO, P.;
- STAS, M.;
- DE WEVER, I.;
- CORNELIS, A.;
- VAN DEN BERGHE, H.
Publication type:
Article
An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation.
Published in:
Clinical Genetics, 1989, v. 36, n. 6, p. 451, doi. 10.1111/j.1399-0004.1989.tb03375.x
By:
- Buttiens, M.;
- Fryns, J. P.;
- Berghe, H. van den
Publication type:
Article
The motivation of at-risk individuals and their partners in deciding for or against predictive testing for Huntington's disease.
Published in:
Clinical Genetics, 1989, v. 35, n. 1, p. 29, doi. 10.1111/j.1399-0004.1989.tb02902.x
By:
- Evers-Kiebooms, G.;
- Swerts, A.;
- Cassiman, J. J.;
- Berghe, H. Van Den
Publication type:
Article
Fragile (X) syndrome: a study of the psychological profile in 23 prepubertal patients.
Published in:
Clinical Genetics, 1987, v. 32, n. 3, p. 179, doi. 10.1111/j.1399-0004.1987.tb03351.x
By:
- Borghgraef, M.;
- Fryns, J. P.;
- Dlelkens, A.;
- Pyck, K.;
- Berghe, H. Van Den
Publication type:
Article
Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5)(p13.1 → p15.3).
Published in:
Clinical Genetics, 1987, v. 32, n. 1, p. 49, doi. 10.1111/j.1399-0004.1987.tb03323.x
By:
- Kleczkowska, A.;
- Fryns, J. P.;
- Moerman, Ph.;
- Vandenberghe, K.;
- Berghe, H. Van den
Publication type:
Article
Proximal duplication of the long arm of chromosome 10 (10q11.2 → 10q22): a distinct clinical entity.
Published in:
Clinical Genetics, 1987, v. 32, n. 1, p. 61, doi. 10.1111/j.1399-0004.1987.tb03325.x
By:
- Fryns, J. P.;
- Kleczkowska, A.;
- Igodt-Ameye, L.;
- Berghe, H. Van den
Publication type:
Article
The Brachmann-de Lange syndrome in two siblings of normal parents.
Published in:
Clinical Genetics, 1987, v. 31, n. 6, p. 413, doi. 10.1111/j.1399-0004.1987.tb02835.x
By:
- FRYNS, J. P.;
- Dereymaeker, A. M.;
- Hoefnagels, M.;
- D'Hondt, F.;
- Mertens, G.;
- Berghe, H. van den
Publication type:
Article
Unusual in vivo rearrangements of the Y-chromosome in two males.
Published in:
Clinical Genetics, 1987, v. 31, n. 3, p. 132, doi. 10.1111/j.1399-0004.1987.tb02783.x
By:
- Fryns, J. P.;
- Kleczkowska, A.;
- Lemmens, P.;
- Berghe, H. Van den
Publication type:
Article
Tetraploidy with hydrops fetalis, cystic nuchal hygroma and 90, XX karyotype.
Published in:
Clinical Genetics, 1987, v. 31, n. 3, p. 158, doi. 10.1111/j.1399-0004.1987.tb02788.x
By:
- FRYNS, J. P.;
- Vandenberghe, K.;
- Moerman, F.;
- Kleczkowska, A.;
- Berghe, H. Van den
Publication type:
Article
Trisomy (18q) and tetrasomy (18p) resulting from isochromosome formation.
Published in:
Clinical Genetics, 1986, v. 30, n. 6, p. 503, doi. 10.1111/j.1399-0004.1986.tb01918.x
By:
- Kleczkowska, A.;
- Fryns, J. P.;
- Buttiens, M.;
- Bisschop, F. de;
- Emmery, L.;
- Berghe, H. Van den
Publication type:
Article
A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patients.
Published in:
Clinical Genetics, 1986, v. 30, n. 4, p. 315, doi. 10.1111/j.1399-0004.1986.tb00613.x
By:
- Fryns, J. P.;
- Kleczkowska, A.;
- Dereymaeker, A.;
- Hoefnagels, M.;
- Heremans, G.;
- Marien, J.;
- Berghe, H. VAN DEN
Publication type:
Article
Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1.
Published in:
Clinical Genetics, 1986, v. 30, n. 4, p. 255, doi. 10.1111/j.1399-0004.1986.tb00605.x
By:
- Fryns, J. P.;
- Kleczkowska, A.;
- Buttiens, M.;
- Marien, P.;
- Berghe, H. VAN DEN
Publication type:
Article
An asymmetric type of chondrodysplasia in an adult male.
Published in:
Clinical Genetics, 1986, v. 30, n. 4, p. 324, doi. 10.1111/j.1399-0004.1986.tb00614.x
By:
- Fryns, J. P.;
- Berghe, H. VAN DEN
Publication type:
Article
Gonadoblastoma and Y-chromosome fluorescence.
Published in:
Clinical Genetics, 1986, v. 29, n. 4, p. 311, doi. 10.1111/j.1399-0004.1986.tb01259.x
By:
- Lukusa, T.;
- Fryns, J. P.;
- Berghe, H. van den
Publication type:
Article
The Borjeson-Fbrssman-Lehmann syndrome.
Published in:
Clinical Genetics, 1986, v. 29, n. 4, p. 317, doi. 10.1111/j.1399-0004.1986.tb01260.x
By:
- Dereymaeker, A. M.;
- Fryns, J. P.;
- Hoefnagels, M.;
- Heremans, G.;
- Marien, J.;
- Berghe, H. van den
Publication type:
Article
Population cytogenetics of autosomal fragile sites.
Published in:
Clinical Genetics, 1986, v. 29, n. 2, p. 96, doi. 10.1111/j.1399-0004.1986.tb01229.x
By:
- Petit, P.;
- Fryns, J. P.;
- Berghe, H. van den;
- Hecht, F.
Publication type:
Article
Mental retardation with pterygia, shortness and distinct facial appearance A new MCA/MR syndrome.
Published in:
Clinical Genetics, 1985, v. 28, n. 6, p. 550, doi. 10.1111/j.1399-0004.1985.tb00425.x
By:
- Haspeslagh, M.;
- Fryns, J. P.;
- Mûelenaere, A. de;
- Schautteet, L.;
- Eeckhoutte, I. van;
- Berghe, H. van den
Publication type:
Article
Partial 8p trisomy due to interstitial duplication: karyotype: 46, XX, inv dup(8) (p21.1→p22).
Published in:
Clinical Genetics, 1985, v. 28, n. 6, p. 546, doi. 10.1111/j.1399-0004.1985.tb00424.x
By:
- Fryns, J. P.;
- Kleczkowska, A.;
- Dereymaker, A. M.;
- Hoefnagels, M.;
- Heremans, G.;
- Marien, J.;
- Berghe, H. van den
Publication type:
Article
Effect of balanced X/autosome translocations on sexual and physical development.
Published in:
Clinical Genetics, 1985, v. 27, n. 2, p. 147, doi. 10.1111/j.1399-0004.1985.tb00202.x
By:
- Kleczkowska, A.;
- Fryns, J. P.;
- Vinken, L.;
- Berghe, H. van den
Publication type:
Article
The relative risk for standard 21 trisomy has not increased in young mothers in Belgium, 1960-1978.
Published in:
Clinical Genetics, 1985, v. 27, n. 1, p. 33, doi. 10.1111/j.1399-0004.1985.tb00181.x
By:
- Evers-Kiebooms, G.;
- Vlietinck, R.;
- Berghe, H. van den
Publication type:
Article
Klinefelter syndrome and two fragile X chromosomes.
Published in:
Clinical Genetics, 1984, v. 26, n. 5, p. 445, doi. 10.1111/j.1399-0004.1984.tb01086.x
By:
- Fryns, J. P.;
- Kleczkowska, A.;
- Wolfs, I.;
- Berghe, H. VAN DEN
Publication type:
Article
The psychological profile of the fragile X syndrome.
Published in:
Clinical Genetics, 1984, v. 25, n. 2, p. 131, doi. 10.1111/j.1399-0004.1984.tb00474.x
By:
- Fryns, J. P.;
- Jacobs, J.;
- Kleczkowska, A.;
- Berghe, H. van den
Publication type:
Article
Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parents.
Published in:
Clinical Genetics, 1983, v. 24, n. 3, p. 156, doi. 10.1111/j.1399-0004.1983.tb02232.x
By:
- Fryns, J. P.;
- Kleczkowska, A.;
- Verresen, H.;
- Berghe, H. van den
Publication type:
Article
Replication and inactivation of and isodicentric X: presence of an inactive centromere influences the replication patterns.
Published in:
Clinical Genetics, 1983, v. 24, n. 3, p. 180, doi. 10.1111/j.1399-0004.1983.tb02236.x
By:
- Fryns, J. P.;
- Petit, P.;
- Klechzkowska, A.;
- Berghe, H. van den
Publication type:
Article
X-chromosome polysomy in the female: personal experience and review of the literature.
Published in:
Clinical Genetics, 1983, v. 23, n. 5, p. 341, doi. 10.1111/j.1399-0004.1983.tb00443.x
By:
- Fryns, J. P.;
- Kleczkowska, A.;
- Petit, P.;
- Berghe, H. van den
Publication type:
Article
Prenatal diagnosis of campomelic dwarfism.
Published in:
Clinical Genetics, 1981, v. 19, n. 3, p. 199, doi. 10.1111/j.1399-0004.1981.tb00696.x
By:
- Fryns, J. P.;
- Berghe, K. van den;
- Assche, A. van;
- Berghe, H. van den
Publication type:
Article
'Adult' form of polycystic kidney disease in neonates.
Published in:
Clinical Genetics, 1979, v. 15, n. 2, p. 205, doi. 10.1111/j.1399-0004.1979.tb01765.x
By:
- Fryns, J. P.;
- Berghe, H. Van Den
Publication type:
Article
Short stature, craniofacial dysmorphism and dento-skeletal abnormalities in a large kindred.
Published in:
Clinical Genetics, 1977, v. 12, n. 5, p. 263, doi. 10.1111/j.1399-0004.1977.tb00939.x
By:
- Parloir, C.;
- Fryns, J. P.;
- Deroover, J.;
- Lebas, E.;
- Goffaux, P.;
- Berghe, H. van den
Publication type:
Article
Feasibility of peripheral blood progenitor cell harvest and transplantation in patients with poor-risk myelodysplastic syndromes.
Published in:
British Journal of Haematology, 1996, v. 92, n. 2, p. 351, doi. 10.1046/j.1365-2141.1996.d01-1479.x
By:
- Demuynck, H.;
- Delforge, M.;
- Verhoef, G. E. G.;
- Zachee, P.;
- Vandenberghe, P.;
- Van Den Berghe, H.;
- Boogaerts, M. A.
Publication type:
Article
Trisomy 12 is uncommon in typical chronic lymphocytic leukaemias.
Published in:
British Journal of Haematology, 1994, v. 87, n. 3, p. 523, doi. 10.1111/j.1365-2141.1994.tb08307.x
By:
- Criel, A.;
- Wlodarska, I.;
- Meeus, P.;
- Stul, M.;
- Louwagie, A.;
- Hoof, A. Van;
- Hidajat, M.;
- Mecucci, C.;
- Berghe, H. Van den
Publication type:
Article
Book Reviews.
Published in:
British Journal of Haematology, 1992, v. 82, n. 4, p. 785, doi. 10.1111/j.1365-2141.1992.tb06969.x
By:
- Roberts, B. E.;
- van den Berghe, H.
Publication type:
Article

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