J. Wraith

发表

Velo‐cardio‐facial syndrome presenting as holoprosencephaly

M. Super, G. H. Watson, J. Wraith, 1985, Clinical genetics.

Homozygous loss of a cysteine residue in the glucocerebrosidase gene results in Gaucher's disease with a hydropic phenotype

F. Stewart, C. Thornton, H. Church, 2004, European Journal of Human Genetics.

Newborn screening for mucopolysaccharidoses: opinions of patients and their families

M. Delatycki, V. Collins, J. Wraith, 2007, Clinical genetics.

Magnetic resonance imaging of the brain, neck and cervical spine in mild Hunter's syndrome (mucopolysaccharidoses type II).

D. Hughes, J. Wraith, V. Parsons, 1994, Clinical radiology.

MRI of the brain and craniocervical junction in Morquio's disease

J. Jenkins, D. Hughes, J. Wraith, 1997, Neuroradiology.

A terminal deletion of 11 q

C. Mpofu, C. Schwarz, J. Wraith, 2022 .

Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing clinicians

M. Delatycki, J. E. Wraith, J. Fraser, 2002, Clinical genetics.

Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease

B. Byrne, H. Mandel, N. Leslie, 2009, Genetics in Medicine.

Optic atrophy in association with cobalamin C (cblC) disease

I. C. Lloyd, S. Beatty, N. Patton, 2000, Ophthalmic genetics.