WDR45B‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome by Suleiman, J., Allingham‐Hawkins, D., Hashem, M., Shamseldin, H.E., Alkuraya, F.S., El‐Hattab, A.W.

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Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000 by Creighton, S, Almqvist, EW, MacGregor, D, Fernandez, B, Hogg, H, Beis, J, Welch, JP, Riddell, C, Lokkesmoe, R, Khalifa, M, MacKenzie, J, Sajoo, A, Farrell, S, Robert, F, Shugar, A, Summers, A, Meschino, W, Allingham-Hawkins, D, Chiu, T, Hunter, A, Allanson, J, Hare, H, Schween, J, Collins, L, Sanders, S, Greenberg, C, Cardwell, S, Lemire, E, MacLeod, P, Hayden, MR

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Prevalence and penetrance of BRCA1 and BRCA2 gene Mutations in unselected Ashkenazi Jewish women with breast cancer by WARNER, E, FOULKES, W, DI PROSPERO, L, CONTIGA, V, SERRUYA, C, KLEIN, M, MOSLEHI, R, HONEYFORD, J, LIEDE, A, GLENDON, G, BRUNET, J.-S, NAROD, S, GOODWIN, P, MESCHINO, W, BLONDAL, J, PATERSON, C, OZCELIK, H, GOSS, P, ALLINGHAM-HAWKINS, D, HAMEL, N

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FRAXE expansion is not a common etiological factor among developmentally delayed males by ALLINGHAM-HAWKINS, D. J, RAY, P. N

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Somatic cell hybridization of Roberts Syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes by ALLINGHAM-HAWKINS, D. J, TOMKINS, D. J

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Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry by Allingham-Hawkins, Diane J., McGlynn-Steele, Leslie K., Brown, Charlotte A., Sutherland, Joanne, Ray, Peter N.

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Compound heterozygosity for the achondroplasia-hypochondroplasia FGFR3 mutations: Prenatal diagnosis and postnatal outcome by Chitayat, David, Fernandez, Bridget, Gardner, Allen, Moore, Lori, Glance, Phyllis, Dunn, Michael, Chun, Kathy, Sgro, Michael, Ray, Peter, Allingham-Hawkins, Dianne

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Eighth International Workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997 by Holden, Jeanette J.A., Percy, Maire, Allingham-Hawkins, Diane, Brown, W. Ted, Chiurazzi, Pietro, Fisch, Gene, Gane, Louise, Gunter, Chris, Hagerman, Randi, Jenkins, Edmund C., Kooy, R. Frank, Lubs, Herbert A., Murray, Anna, Neri, Giovanni, Schwartz, Charles, Tranebjaerg, Lisbeth, Villard, Laurent, Willems, Patrick J.

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Compound Heterozygosity for the Achondroplasia-Hypochondroplasia FGFR3 Mutations: Prenatal Diagnosis and Postnatal Outcome by Chitayat, D, Fernandez, B, Gardner, A, Moore, L, Glance, P, Dunn, M, Chun, K, Sgro, M, Ray, P, Allingham-Hawkins, D

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Fragile X premutation is a significant risk factor for premature ovarian failure : The international collaborative POF in fragile X study : Preliminary data: X-linked mental retard... by ALLINGHAM-HAWKINS, D. J, BABUL-HIRJI, R, JENKINS, E. C, BROWN, W. T, HOWARD-PEEBLES, P. N, BECCHI, C, CUMMINGS, E, FALLON, L, SEITZ, S, BLACK, S. H, VIANNA-MORGANTE, A. M, COSTA, S. S, CHITAYAT, D, OTTO, P. A, MINGRONI-NETTO, R. C, MURRAY, A, WEBB, J, MACSWINNEY, F, DENNIS, N, JACOBS, P. A, SYRROU, M, GEORGIOU, I, PATSALIS, P. C, HOLDEN, J. J. A, GIOVANNUCCI UZIELLI, M. L, GUARDUCCI, S, LAPI, E, CECCONI, A, RICCI, U, RICOTTI, G, BIONDI, C, SCARSELLI, B, VIERI, F, YANG, K. T, LEE, C, HUDSON, R, GORWILL, H, NOLIN, S. L, GLICKSMAN, A

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