S. Holder

No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate.

R. Winter, S. Malcolm, G. Vintiner, 1992, Journal of medical genetics.

Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate.

R. Winter, S. Holder, S. Malcolm, 1992, Journal of medical genetics.

Isolated non‐compaction of the ventricular myocardium: prenatal diagnosis and natural history

S. Holder, H. M. Gardiner, A. Karatza, 2003, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Trisomy 17p10‐p12 resulting from a supernumerary marker chromosome derived from chromosome 17: molecular analysis and delineation of the phenotype

P. Stankiewicz, L. Potocki, J. Lupski, 2001, Clinical genetics.

Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies.

R. Winter, S. Malcolm, G. Vintiner, 1993, Journal of medical genetics.

Partial trisomy 3q causing mild Cornelia de Lange phenotype.

M. Baraitser, S. Holder, L. Butler, 1994, Journal of medical genetics.

Appendiceal Endometriosis and Ectopic Pregnancy Occurring Simultaneously.

Anat Chemerinski, D. Shah, D. Lubin, 2018, Obstetrics and gynecology.

Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver–Russell syndrome

D. Mackay, E. Wakeling, D. Robinson, 2008, Journal of Medical Genetics.

Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype.

P. Scambler, R. Winter, S. Holder, 1993, Journal of medical genetics.

Otopalatodigital syndrome type II.

R. Winter, S. Holder, 1993, Journal of medical genetics.

Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies

K. Lakhoo, S. Bhattacharya, P. Syrris, 2001, Journal of medical genetics.

Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype.

P. Scambler, R. Winter, S. Holder, 1993, Journal of medical genetics.

The protean manifestations of RASA1 gene mutation

S. Wakelin, J. Carton, S. Holder, 2019, Clinical and experimental dermatology.