New Articles from Clinical Genetics is Now Available

September 20, 2007

Clinical Genetics articles are now available by subscription only.

Reviews
“The role of common genetic risk variants in Parkinson disease” by E-K Tan.

HotSpots
“Genetics of Noonan syndrome – a new gene, and the search is still on” by RA Stein.

Letters to the Editor
“Prenatal diagnosis of Miller-Dieker syndrome by ultrasound and molecular cytogenetic analysis” by Elisabetta Lenzini, Giuseppina D’Ottavio, Angelo Città, Daniela Gambel Benussi, Vincenzo Petix, Vanna Pecile.

Short Reports
“Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome” by E Engenheiro, J Saraiva, I Carreira, L Ramos, HH Ropers, E Silva, N Tommerup and Z Tümer.

Letters to the Editor
“Parkin polymorphisms: risk for Parkinson’s disease in Indian population” by A Biswas, M Maulik, SK Das, Indian Genome Variation Consortium, K Ray, J Ray.

Short Reports
“A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome” by B Auber, P Burfeind, S Herold, K Schoner, G Simson, R Rauskolb and H Rehder.
“Cytogenetic and molecular characterization of the derivative Y chromosome: a case study of an azoospermic patient” by T Roovere, M Peters, N Horelli-Kuitunen, T Mölter-Väär, M Punab, S Rootsi, O Poolamets and A Salumets.

Letters to the Editor
“The homozygous deletion of the 3′ enhancer of the SHOX gene causes Langer mesomelic dysplasia” by R Bertorelli, L Capone, F Ambrosetti, L Garavelli, L Varriale, V Mazza, I Stanghellini, A Percesepe, A Forabosco.