Planning for a Healthy Baby: A Guide to Genetic and Environmental Risks

Por Fitzsimmons, J S
Publicado em 1988

The teaching of human genetics in schools.

Por Fitzsimmons, J S
Publicado em 1983

Classroom teaching in genetics and birth defects: the Nottingham experience.

Por Fitzsimmons, J S
Publicado em 1985

Uncommon complication of anaphylactoid purpura.

Por Fitzsimmons, J. S.
Publicado em 1968

Laryngeal stridor and respiratory obstruction associated with meningomyelocele.

Por Fitzsimmons, J. S.
Publicado em 1965

Cutis marmorata telangiectatica congenita or congenital generalized phlebectasia.

Por Fitzsimmons, J S, Starks, M
Publicado em 1970

A family study of hidradenitis suppurativa.

Por Fitzsimmons, J S, Guilbert, P R
Publicado em 1985

Spastic paraplegia associated with brachydactyly and cone shaped epiphyses.

Por Fitzsimmons, J S, Guilbert, P R
Publicado em 1987

The role of thiol groups in the multiple forms of an invertebrate creatine kinase.

Por Doherty, M D, Fitzsimmons, J A
Publicado em 1970

Principles of lithogenesis /

Por Strakhov, Nikolai Mikhailovich, Fitzsimmons, J. Paul.
Publicado em 1967.

Familial hidradenitis suppurativa: evidence in favour of single gene transmission.

Por Fitzsimmons, J S, Fitzsimmons, E M, Gilbert, G
Publicado em 1984

Genetic heterogeneity in the Freeman-Sheldon syndrome: two adults with probable autosomal recessive inheritance

Por Fitzsimmons, J S, Zaldua, V, Chrispin, A R
Publicado em 1984

Congenital discoid lupus in the newborn.

Por Fitzsimmons, J S, Crawford, M J, Reeves, W G
Publicado em 1977

Antenatal diagnosis of trisomy 13 with unexpected increase in alpha-feto protein.

Por Fitzsimmons, J S, Filshie, G M, Hill, A S, Kime, R
Publicado em 1976

Roberts syndrome: clinical and cytogenetic aspects

Por Mann, N P, Fitzsimmons, J, Fitzsimmons, E, Cooke, P
Publicado em 1982

Letter: Serum alpha-fetoprotein in cystic fibrosis.

Por Fitzsimmons, J S, Smith, N, Hiller, E J, Wynne, J
Publicado em 1975

Familial spastic paraplegia, bilateral sensorineural deafness, and intellectual retardation associated with a progressive nephropathy.

Por Fitzsimmons, J S, Watson, A R, Mellor, D, Guilbert, P R
Publicado em 1988

Parental consanguinity and the Majewski syndrome.

Por Black, I L, Fitzsimmons, J, Fitzsimmons, E, Thomas, A J
Publicado em 1982

Location of the gene for 21-hydroxylase deficiency.

Por Pucholt, V, Fitzsimmons, J S, Gelsthorpe, K, Reynolds, M A, Milner, R D
Publicado em 1980

Poliomyelitis surveillance: the model used in India for polio eradication.

Por Banerjee, K., Hlady, W. G., Andrus, J. K., Sarkar, S., Fitzsimmons, J., Abeykoon, P.
Publicado em 2000