A citation-based method for searching scientific literature

A Cooke, J Tolmie, W Darlington, E Boyd, R Thomson, M A Ferguson-Smith. J Med Genet 1987
Times Cited: 34

List of shared articles

Times cited

Deletion of 16q with prolonged survival and unusual radiographic manifestations.
A C Casamassima, R M Klein, P L Wilmot, P Brenholz, L R Shapiro. Am J Med Genet 1990

Silver-Russell syndrome and ring chromosome 7.
E L Wakeling, M Hitchins, P Stanier, D Monk, G E Moore, M A Preece. J Med Genet 2000

Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)
D A Bessant, A M Payne, B E Snow, G Antiño, S Q Mehdi, A C Bird, D P Siderovski, S S Bhattacharya. J Med Genet 2000

Clinical and molecular cytogenetic studies of a large de novo interstitial deletion 16q11.2-16q21 including the putative transcription factor gene SALL1.
H Knoblauch, G Thiel, S Tinschert, H Körner, C Tennstedt, R Chaoui, J Kohlhase, C Dixkens, C Blanck. J Med Genet 2000

No linkage or association of the IL-4Ralpha gene Q576R mutation with atopic asthma in Italian families.
C Patuzzo, E Trabetti, G Malerba, L C Martinati, A L Boner, L Pescollderungg, G Zanoni, P F Pignatti. J Med Genet 2000

Familial Wilms tumour resulting from WT1 mutation: intronic polymorphism causing artefactual constitutional homozygosity.
K Pritchard-Jones, N Rahman, M Gerrard, D Variend, L King-Underwood. J Med Genet 2000