I. Young

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Mild form of Hunter's syndrome: clinical delineation based on 31 cases.

P. Harper, I. Young, 1982, Archives of disease in childhood.

RECURRENCE RISK IN OSTEOGENESIS IMPERFECTA CONGENITA

P. Harper, I. Young, 1980, The Lancet.

Hereditary distal spinal muscular atrophy with vocal cord paralysis.

P. Harper, I. Young, 1980, Journal of neurology, neurosurgery, and psychiatry.

Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfecta

M. Pembrey, I. Young, E. Thompson, 1989, Clinical genetics.

Localization of plasminogen activator in kidney tissue.

R. Holemans, I. Young, J. G. Johnson, 1966, Laboratory investigation; a journal of technical methods and pathology.

THE NATURAL HISTORY OF THE SEVERE FORM OF HUNTER'S SYNDROME: A STUDY BASED ON 52 CASES

I. Young, P. Harper, 1983, Developmental medicine and child neurology.

Down syndrome and maternal age in South Glamorgan.

R. Newcombe, Glamorgan, I. Young, 1980, Journal of medical genetics.

Down syndrome and maternal age in South

R. Newcombe, Glamorgan, I. Young, 2022 .

Incidence of Hunter's syndrome

P. Harper, I. Young, 2004, Human Genetics.

A clinical and genetic study of Hunter's syndrome. 2 Differences between the mild and severe forms

R. Newcombe, P. Harper, I. Young, 1982, Journal of medical genetics.

High incidence of Meckel's syndrome in Gujarati Indians.

I. Young, M. Clarke, A. Rickett, 1985, Journal of medical genetics.

An unusual form of familial acrocephalosyndactyly.

P. Harper, I. Young, 1982, Journal of medical genetics.

Anunusual formoffamilial acrocephalosyndactyly

I. Young, P. Harper, 1982 .

Carrier detection in Hunter syndrome.

P. Harper, I. Young, F. Wusteman, 1983, American journal of medical genetics.

Low segregation ratios in autosomal recessive disorders.

I. Young, S. Bundey, 1993, Journal of medical genetics.

A clinical and genetic study of Hunter's syndrome. 1 Heterogeneity

R. Newcombe, P. Harper, I. Young, 1982, Journal of medical genetics.

Long‐term complications in Hunter's syndrome

I. Young, P. Harper, 1979, Clinical genetics.

Amniotic bands in connective tissue disorders.

M. Pembrey, E. Thompson, I. Young, 1985, Archives of disease in childhood.

Weill‐Marchesani syndrome in mother and son

A. Fielder, I. Young, T. Casey, 1986, Clinical genetics.

A clinical andgenetic study ofHunter's syndrome. 1Heterogeneity

R. Newcombe, P. Harper, I. Young, 1982 .

Psychosocial problems in Hunter's syndrome.

P. Harper, I. Young, 1981, Child: care, health and development.

Autosomal recessive or sex linked recessive: a counselling dilemma.

T. Grimm, I. Young, Z. Nugent, 1986, Journal of medical genetics.

Desbuquois syndrome

P. Maroteaux, I. Young, V. Stanescu, 2005, European Journal of Pediatrics.

Amniotic bandsinconnective tissue disorders

M. Pembrey, E. Thompson, I. Young, 1985 .

Cranioectodermal dysplasia (Sensenbrenner's syndrome).

I. Young, 1989, Journal of medical genetics.

Smith-Lemli-Opitz syndrome. II: A disorder of the fetal adrenals?

I. Young, I. Young, P. Mckeever, 1990, Journal of medical genetics.

The Coffin-Lowry syndrome.

I. Young, I. Young, 1988, Journal of medical genetics.

Mild form of Hunter's syndrome: clinical delineation based on 31 cases.

P. Harper, I. Young, 1982, Archives of disease in childhood.