Fragile X syndrome without CCG amplification has an FMR1 deletion von Gedeon, A.K., Baker, E., Robinson, H., Partington, M.W., Gross, B., Manca, A., Korn, B., Poustka, A., Yu, S., Sutherland, G.R., Mulley, J.C.

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Confirmation of early menopause in fragile X carriers von Partington, M.W., Moore, D.Y., Turner, G.M.

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CORRESPONDENCE von FINER, B.L., PARTINGTON, M.W.

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CORRESPONDENCE von FINER, B.L., PARTINGTON, M.W.

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AN ILLNESS OF INFECTION IN CHICKENPOX von Partington, M.W.

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TIME OF RECURRENCE OR CURE OF TUMOURS IN CHILDHOOD von Partington, M.W.

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ACTIVITY OF THE ANTI-HISTAMINE DRUGS von Partington, M.W.

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Erratum von Sherman, S.L., Jacobs, P.A., Morton, N.E., Froster-Iskenius, U., Howard-Peebles, P.N., Nielsen, K.B., Partington, M.W., Sutherland, G.R., Turner, G., Watson, M.

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The relation of plasma tyrosine level to weight gain of premature infants von Partington, M.W., Mathews, John

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Pediatrics-Anticonvulsant Therapy von McGlannan, Frances, DeLuca, K., Masotti, R.E., Partington, M.W.

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Localisation of the gene for X-linked reticulate pigmentary disorder with systemic manifestations (PDR), previously known as X-linked cutaneous amyloidosis von Gedeon, A. K., Mulley, J. C., Kozman, H., Donnelly, A., Partington, M. W.

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Clinical and linkage study of a large family with simple ectopia lentis linked to FBN1 von Edwards, M. J., Challinor, C. J., Colley, P. W., Roberts, J., Partington, M. W., Hollway, G. E., Kozman, H. M., Mulley, J. C.

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Clinical Rounds von Bryans, A.M., Varga, E., Wollin, D.G., Purvis, J.R., Partington, M.W., Delahaye, D.J., Alexander, D.S., Partington, M.W.

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Biochemical changes caused by decellularization may compromise mechanical integrity of tracheal scaffolds von Partington, L., Mordan, N.J., Mason, C., Knowles, J.C., Kim, H-W., Lowdell, M.W., Birchall, M.A., Wall, I.B.

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Stem Cell-Based Tissue-Engineered Laryngeal Replacement von Ansari, T, Lange, P, Southgate, A, Greco, K, Carvalho, C, Partington, L, Bullock, A, MacNeil, S, Lowdell, M.W, Sibbons, P.D, Birchall, M.A

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