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Journal of Medical Genetics|July 25, 1998
Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotypeA K Ryan, K Bartlett, P Clayton, et al.
Journal of Medical Genetics|December 10, 2002
Comparison of genetic services with and without genetic registers: knowledge, adjustment, and attitudes about genetic counselling among probands referred to three genetic clinicsC Wright, L Kerzin-Storrar, P R Williamson, et al.
The British Journal of Ophthalmology|August 1, 1997
Anterior segment dysgenesis in mosaic Turner syndromeI C Lloyd, P M Haigh, J Clayton-Smith, et al.
Plos One|July 23, 2013
Interactions between blood-borne Streptococcus pneumoniae and the blood-brain barrier preceding meningitisFederico Iovino, Carlos J Orihuela, Henk E Moorlag, et al.
Brain : a Journal of Neurology|November 10, 2001
Abnormal corticospinal function but normal axonal guidance in human L1CAM mutationsC B Dobson, F Villagra, G J Clowry, et al.
Journal of Medical Genetics|December 24, 1998
Costello syndrome: two cases with embryonal rhabdomyosarcomaB Kerr, O B Eden, R Dandamudi, et al.
Ophthalmology|May 18, 1999
A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophyH Stewart, G C Black, D Donnai, et al.
Clinical Genetics|March 5, 1999
X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisationH Woffendin, T Jakins, M Jouet, et al.
Cellular Microbiology|March 1, 2013
Signalling or binding: the role of the platelet-activating factor receptor in invasive pneumococcal diseaseFederico Iovino, Matthijs C Brouwer, Diederik van de Beek, et al.
Frontiers in Microbiology|August 9, 2020
Combined Transcriptome Sequencing of Mycoplasma hyopneumoniae and Infected Pig Lung Tissue Reveals Up-Regulation of Bacterial F1-Like ATPase and Down-Regulation of the P102 Cilium Adhesin in vivoTjerko Kamminga, Nirupama Benis, Vitor Martins Dos Santos, et al.
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