Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral developmentBHOJ, Elizabeth J; RAMOS, Purita; VANHOUTTEGHEM, Amandine et al.European journal of human genetics. 2011, Vol 19, Num 5, pp 540-546, issn 1018-4813, 7 p.Article

Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart DiseaseRICHARDS, Ashleigh A; JAECKLE SANTOS, Lane; NICHOLS, Haley A et al.Pediatric research. 2008, Vol 64, Num 4, pp 358-363, issn 0031-3998, 6 p.Article

The phenotype of short stature homeobox gene (SHOX) deficiency in childhood : Contrasting children with leri-weill dyschondrosteosis and turner syndromeROSS, Judith L; KOWAL, Karen; QUIGLEY, Charmian A et al.The Journal of pediatrics. 2005, Vol 147, Num 4, pp 499-507, issn 0022-3476, 9 p.Article

Complete SHOX deficiency causes Langer mesomelic dysplasiaZINN, Andrew R; FANGLIN WEI; LING ZHANG et al.American journal of medical genetics. 2002, Vol 110, Num 2, pp 158-163, issn 0148-7299Article

Lagomorphs (rabbits, pikas and hares) do not use telomere-directed replicative aging in vitroFORSYTH, Nicholas R; ELDER, Frederick F. B; SHAY, Jerry W et al.Mechanisms of ageing and development. 2005, Vol 126, Num 6-7, pp 685-691, issn 0047-6374, 7 p.Article