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Journal of Medical Genetics|April 1, 1994
Genetic heterogeneity in Rieger eye malformationE Legius, C E de Die-Smulders, F Verbraak, et al.
Haematologica|January 12, 2000
Two cases of myeloid disorders and a t(8;12) (q12;p13)J M Hernández, M B González, J L García, et al.
The Journal of Biological Chemistry|February 25, 1988
The molecular organization of human alpha 2-macroglobulin. An immunoelectron microscopic study with monoclonal antibodiesE Delain, M Barray, J Tapon-Bretaudiere, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
A novel MSX1 mutation in hypodontiaS De Muynck, E Schollen, G Matthijs, et al.
American Journal of Human Genetics|November 9, 2000
Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32C R Jamieson, J P Fryns, J Jacobs, et al.
Annales De Genetique|February 13, 2001
Cryptic translocation t(5;18) in familial mental retardationA Vogels, K Devriendt, J R Vermeesch, et al.
British Journal of Haematology|December 3, 1999
Characterization of 12p molecular events outside ETV6 in complex karyotypes of acute myeloid malignanciesR La Starza, M Stella, N Testoni, et al.
The Journal of General Physiology|December 1, 1988
Cytoplasmic free calcium, myosin light chain phosphorylation, and force in phasic and tonic smooth muscleB Himpens, G Matthijs, A V Somlyo, et al.
Blood|March 1, 1997
A new subtype of pre-B acute lymphoblastic leukemia with t(5;12)(q31q33;p12), molecularly and cytogenetically distinct from t(5;12) in chronic myelomonocytic leukemiaI Wlodarska, A Aventín, J Inglés-Esteve, et al.
Acta Neuropathologica|February 7, 1998
Immature teratoma of the pineal gland with isochromosome 12pP Dal Cin, A P Dei Tos, H Qi, et al.
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