Foulds, Dr Nicola Clare
BSc, PhD, MBChB, MRCP
Speciality
Clinical Genetics
Sub-speciality
Dysmorphology, metabolic genetics
Training and Education
BSc Biochemistry and Pharmacology, PhD University of Cambridge, Institute for Biotechnology. MBChB Bristol 1993, trained in paediatrics. Trained on London rotational scheme in Clinical Genetics.
Experience
Dr Foulds has worked for Southampton University Hospitals Trust since September 2004.
Research
Foulds N C, Walpole I, Mansour S, Elmslie F V. Carbimazole Embryopathy: An Emerging Phenotype. Am J Med Genet 2005.132A(2): 130-135.
Mercer C, Gilbert R, Loughlin S, Foulds N. Patient with an EYA1 mutation with features of branchio-oto-renal and Oto-facio-cervical syndrome. Clin Dysmorphol.2006 Oct; 15(4):211-2
Turner C, Emery H, Howarth R, Yearwood C, Cross E, Duncan P, Harvey J, Foulds N. Detection of 53 FBN1 mutations (41 novel and 12 recurrent) and genotype-phenotype correlations in 113 unrelated probands referred with marfan syndrome or a related fbrillinopathy. Am J Med Genet. In Press.