Fitzsimmons JS - Search Results

1

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

Fitzsimmons JS, Watson AR, Mellor D, Guilbert PR. Fitzsimmons JS, et al. J Med Genet. 1988 Mar;25(3):168-72. doi: 10.1136/jmg.25.3.168. J Med Genet. 1988. PMID: 3351903 Free PMC article.

2

Spastic paraplegia associated with brachydactyly and cone shaped epiphyses.

Fitzsimmons JS, Guilbert PR. Fitzsimmons JS, et al. J Med Genet. 1987 Nov;24(11):702-5. doi: 10.1136/jmg.24.11.702. J Med Genet. 1987. PMID: 3430547 Free PMC article.

3

A family study of hidradenitis suppurativa.

Fitzsimmons JS, Guilbert PR. Fitzsimmons JS, et al. J Med Genet. 1985 Oct;22(5):367-73. doi: 10.1136/jmg.22.5.367. J Med Genet. 1985. PMID: 2934550 Free PMC article.

4

Evidence of genetic factors in hidradenitis suppurativa.

Fitzsimmons JS, Guilbert PR, Fitzsimmons EM. Fitzsimmons JS, et al. Among authors: fitzsimmons em. Br J Dermatol. 1985 Jul;113(1):1-8. doi: 10.1111/j.1365-2133.1985.tb02037.x. Br J Dermatol. 1985. PMID: 4015966

5

Four brothers with mental retardation, spastic paraplegia and palmoplantar hyperkeratosis. A new syndrome?

Fitzsimmons JS, Fitzsimmons EM, McLachlan JI, Gilbert GB. Fitzsimmons JS, et al. Among authors: fitzsimmons em. Clin Genet. 1983 Apr;23(4):329-35. doi: 10.1111/j.1399-0004.1983.tb01887.x. Clin Genet. 1983. PMID: 6221837

6

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

Fitzsimmons JS, Fitzsimmons EM, Gilbert G. Fitzsimmons JS, et al. Among authors: fitzsimmons em. J Med Genet. 1984 Aug;21(4):281-5. doi: 10.1136/jmg.21.4.281. J Med Genet. 1984. PMID: 6492093 Free PMC article.

7

Familial recurrence of achondroplasia.

Fitzsimmons JS. Fitzsimmons JS. Am J Med Genet. 1985 Nov;22(3):609-13. doi: 10.1002/ajmg.1320220320. Am J Med Genet. 1985. PMID: 4061493

8

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

Fitzsimmons JS, Zaldua V, Chrispin AR. Fitzsimmons JS, et al. J Med Genet. 1984 Oct;21(5):364-8. doi: 10.1136/jmg.21.5.364. J Med Genet. 1984. PMID: 6502650 Free PMC article.

9

Fronto-metaphyseal dysplasia. Further delineation of the clinical syndrome.

Fitzsimmons JS, Fitzsimmons EM, Barrow M, Gilbert GB. Fitzsimmons JS, et al. Among authors: fitzsimmons em. Clin Genet. 1982 Oct;22(4):195-205. doi: 10.1111/j.1399-0004.1982.tb01433.x. Clin Genet. 1982. PMID: 7151303

10

Variable clinical presentation of cutis laxa.

Fitzsimmons JS, Fitzsimmons EM, Guibert PR, Zaldua V, Dodd KL. Fitzsimmons JS, et al. Among authors: fitzsimmons em. Clin Genet. 1985 Oct;28(4):284-95. doi: 10.1111/j.1399-0004.1985.tb00402.x. Clin Genet. 1985. PMID: 4064367

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