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Archives of Disease in Childhood|April 15, 2014
Familial haematuria: when to consider genetic testingJudy Taylor, Frances Flinter
Clinical Journal of the American Society of Nephrology : CJASN|October 2, 2010
The value of clinical criteria in identifying patients with X-linked Alport syndromeHelen Hanson, Helen Storey, Judith Pagan, et al.
Nature Reviews. Genetics|December 3, 2002
Preimplantation genetic diagnosisPeter Braude, Susan Pickering, Frances Flinter, et al.
American Journal of Medical Genetics. Part A|April 10, 2014
Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: further delineation of an emerging syndromeMichiala Cafferkey, Joo Wook Ahn, Frances Flinter, et al.
Journal of the American Society of Nephrology : JASN|January 26, 2013
Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathyJudy Savige, Martin Gregory, Oliver Gross, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2019
Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesisCaroline Pearce, Emma Goettke, Nina Hallowell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2019
Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesisCaroline Pearce, Emma Goettke, Nina Hallowell, et al.
Molecular Cytogenetics|February 26, 2009
A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case reportCaroline Mackie Ogilvie, Joo Wook Ahn, Kathy Mann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 25, 2010
Aortic abnormalities in males with Alport syndromeClifford E Kashtan, Yoav Segal, Frances Flinter, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|September 20, 2005
The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testingCaroline Mackie Ogilvie, Alison Lashwood, Lyn Chitty, et al.
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