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Journal of Medical Genetics|May 1, 1992
Oculoauriculovertebral spectrum and cerebral anomaliesC T Schrander-Stumpel, C E de Die-Smulders, R C Hennekam, et al.Journal of Medical Genetics|May 1, 1992
Tandem duplication of the terminal band of the long arm of chromosome 7 (dir dup (7)(q36----qter))R S Verma, R A Conte, J H PitterJournal of Medical Genetics|September 13, 2005
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeM A Parisi, D Doherty, M L Eckert, et al.Journal of Medical Genetics|March 4, 2005
The genetics of schizophrenia and bipolar disorder: dissecting psychosisN Craddock, M C O'Donovan, M J OwenJournal of Medical Genetics|March 4, 2005
Association of partial AZFc region deletions with spermatogenic impairment and male infertilityA Ferlin, A Tessari, F Ganz, et al.Journal of Medical Genetics|March 4, 2005
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophyV Cenni, P Sabatelli, E Mattioli, et al.Journal of Medical Genetics|March 4, 2005
Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairsM Y M Ng, T Andrew, T D Spector, et al.Journal of Medical Genetics|March 4, 2005
Association of oestrogen receptor alpha gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of boneO M E Albagha, U Pettersson, A Stewart, et al.Journal of Medical Genetics|June 1, 1979
Two balanced translocations in three generations of a pedigree: t(7;10) (q11;q22) and t(14;21) (14qter to cen to 21qter)1H N Bass, R S SparkesJournal of Medical Genetics|May 3, 2005
Evidence of an association between genetic variation of the coactivator PGC-1beta and obesityG Andersen, L Wegner, K Yanagisawa, et al.Pageof 649