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American Journal of Human Genetics|March 1, 1995
Clinical and molecular characterization of patients with distal 11q deletionsL A Penny, M Dell'Aquila, M C Jones, et al.
Journal of Medical Genetics|July 9, 2009
Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangementsB I Dimitrov, T de Ravel, J Van Driessche, et al.
Human Genetics|September 1, 1990
Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian familiesH Cuppens, E Legius, P Cabello, et al.
Journal of Medical Genetics|February 12, 2002
The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactylyP Debeer, E F P M Schoenmakers, W O Twal, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 14, 2008
Imaging of gynecological disease (3): clinical and ultrasound characteristics of granulosa cell tumors of the ovaryC Van Holsbeke, E Domali, T K Holland, et al.
Journal of Clinical Pathology|June 30, 2009
Triple negative breast cancer: a study from the point of view of basal CK5/6 and HER-1S Pintens, P Neven, M Drijkoningen, et al.
British Journal of Cancer|September 27, 2007
Clinical study investigating the role of lymphadenectomy, surgical castration and adjuvant hormonal treatment in endometrial stromal sarcomaF Amant, A De Knijf, B Van Calster, et al.
Oncology Reports|July 31, 1998
An important subgroup of phyllodes tumors of the breast is characterized by rearrangements of chromosomes 1q and 10qP Polito, P Dal Cin, P Pauwels, et al.
European Journal of Medical Genetics|September 24, 2005
The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patientsG Van Buggenhout, C Van Ravenswaaij-Arts, N Mc Maas, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Mesomelic form of chondrodysplasia and congenital glaucoma associated with de novo translocation (13;18)(q14;q23)B Dimitrov, K Devriendt, N M C Maas, et al.
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