N. Nathwani

Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ

Soo-Mi Park, C. Anderson, M. Dattani, 2016, The Journal of clinical endocrinology and metabolism.

A comparative study between infertile males and patients with Turner syndrome to determine the influence of sex chromosome mosaicism and the breakpoints of structurally abnormal Y chromosomes on phenotypic sex

G. Conway, P. Serhal, J. Delhanty, 2002, Journal of medical genetics.

Antibody Responses to Immunizations in Children with Type I Diabetes Mellitus: a Case-Control Study

M. Eisenhut, A. Chesover, N. Nathwani, 2016, Clinical and Vaccine Immunology.

Cytogenetic and molecular investigations of Y chromosome sequences and their role in Turner syndrome

G. Conway, J. Delhanty, C. Quilter, 1998, Annals of human genetics.

Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD)

L. Metherell, H. Storr, M. Savage, 2014, The Journal of clinical endocrinology and metabolism.

Bacterial colonisation of leg ulcers and its effect on the success rate of skin grafting.

C. Doré, J. Lewis, E. L. Gilliland, 1988, Annals of the Royal College of Surgeons of England.

Transient Broca's aphasia as feature of an extradural abscess.

M. Eisenhut, N. Nathwani, C. Fowler, 2009, Pediatric neurology.