Familial Breast and Ovarian Cancer: Genetics, Screening and Management

Por Huson, S M
Publicado em 2004

The different forms of neurofibromatosis.

Por Huson, S M
Publicado em 1987

Recent developments in the diagnosis and management of neurofibromatosis.

Por Huson, S M
Publicado em 1989

Neurofibromatosis: Phenotype, Natural History and Pathogenesis

Por Huson, Susan M
Publicado em 1993

The First European Symposium on Neurofibromatosis

Por Huson, Susan M
Publicado em 1987

Neurofibromatosis: Phenotype, Natural History and Pathogenesis

Por Huson, Susan M
Publicado em 1987

Anita Harding (1952-95): In Memoriam

Por Poulton, J., Huson, S. M.
Publicado em 1996

A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.

Por Huson, S M, Compston, D A, Harper, P S
Publicado em 1989

Three sibs with phalangeal anomalies, microcephaly, severe mental retardation, and neurological abnormalities.

Por Woods, C G, Crouchman, M, Huson, S M
Publicado em 1992

An exclusion map for Von Recklinghausen neurofibromatosis.

Por Sarfarazi, M, Huson, S M, Edwards, J H
Publicado em 1987

Interstitial deletion of band 3q25.

Por Slavotinek, A M, Huson, S M, Fitchett, M
Publicado em 1997

Instability versus predictability: the molecular diagnosis of myotonic dystrophy.

Por Suthers, G K, Huson, S M, Davies, K E
Publicado em 1992

Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markers.

Por Upadhyaya, M, Sarfarazi, M, Huson, S M, Harper, P S
Publicado em 1987

A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity.

Por Huson, S M, Compston, D A, Clark, P, Harper, P S
Publicado em 1989

Reply

Por Suthers, Graeme K, Davies, Kay E, Huson, Susan M
Publicado em 1993

Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?

Por Brueton, L A, Huson, S M, Farren, B, Winter, R M
Publicado em 1990

The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome.

Por Huson, S M, Rodgers, C S, Hall, C M, Winter, R M
Publicado em 1990

The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3.

Por Slavotinek, A, Maher, E, Gregory, P, Rowlandson, P, Huson, S M
Publicado em 1997

Neurofibromatoses in clinical practice

Por Ferner, Rosalie E., Huson, Susan M., Evans, D. Gareth R.
Publicado em 2011

Malignant peripheral nerve sheath tumours in inherited disease

Por Evans, D Gareth R, Huson, Susan M, Birch, Jillian M
Publicado em 2012