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Watson syndrome: is it a subtype of type 1 neurofibromatosis?
Allanson JE, Upadhyaya M, Watson GH, Partington M, MacKenzie A, Lahey D, MacLeod H, Sarfarazi M, Broadhead W, Harper PS, et al. Allanson JE, et al. Among authors: partington m. J Med Genet. 1991 Nov;28(11):752-6. doi: 10.1136/jmg.28.11.752. J Med Genet. 1991. PMID: 1770531 Free PMC article.
Non-specific X linked mental retardation.
Kerr B, Turner G, Mulley J, Gedeon A, Partington M. Kerr B, et al. Among authors: partington m. J Med Genet. 1991 Jun;28(6):378-82. doi: 10.1136/jmg.28.6.378. J Med Genet. 1991. PMID: 1870094 Free PMC article. Review.
Is there a fragile(X) negative Martin-Bell syndrome?
Thode A, Laing S, Partington MW, Turner G. Thode A, et al. Among authors: partington mw. Am J Med Genet. 1988 May-Jun;30(1-2):459-71. doi: 10.1002/ajmg.1320300149. Am J Med Genet. 1988. PMID: 3052069 Review.
Rett syndrome in monozygotic twins.
Partington MW. Partington MW. Am J Med Genet. 1988 Mar;29(3):633-7. doi: 10.1002/ajmg.1320290322. Am J Med Genet. 1988. PMID: 3377006
250 results