CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients
Archer, H L, Evans, J, Edwards, S, Colley, J, Newbury-Ecob, R, O’Callaghan, F, Huyton, M, O’Regan, M, Tolmie, J, Sampson, J, Clarke, A, Osborne, J
Published in Journal of medical genetics (01.09.2006)
Published in Journal of medical genetics (01.09.2006)
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Journal Article
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients
Archer, H L, Whatley, S D, Evans, J C, Ravine, D, Huppke, P, Kerr, A, Bunyan, D, Kerr, B, Sweeney, E, Davies, S J, Reardon, W, Horn, J, MacDermot, K D, Smith, R A, Magee, A, Donaldson, A, Crow, Y, Hermon, G, Miedzybrodzka, Z, Cooper, D N, Lazarou, L, Butler, R, Sampson, J, Pilz, D T, Laccone, F, Clarke, A J
Published in Journal of medical genetics (01.05.2006)
Published in Journal of medical genetics (01.05.2006)
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Journal Article
People with MECP2 mutation-positive Rett disorder who converse
Kerr, A. M., Archer, H. L., Evans, J. C., Prescott, R. J., Gibbon, F.
Published in Journal of intellectual disability research (01.05.2006)
Published in Journal of intellectual disability research (01.05.2006)
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Journal Article
Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter
Archer, H.L., Gupta, S., Enoch, S., Thompson, P., Rowbottom, A., Chua, I., Warren, S., Johnson, D., Ledbetter, D.H., Lese-Martin, C., Williams, P., Pilz, D.T.
Published in American journal of medical genetics. Part A (01.07.2005)
Published in American journal of medical genetics. Part A (01.07.2005)
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Journal Article
Wealth Flow and Fertility Decline in Rural Kenya, 1981-92: A Reassessment of the Evidence
Dow, Thomas E., Kekovole, John, Archer, Linda H.
Published in African journal of reproductive health (01.09.1997)
Published in African journal of reproductive health (01.09.1997)
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Journal Article
Early onset seizures and Rett-like features associated with mutations in CDKL5
EVANS, Julie C, ARCHER, Hayley L, WRIGHT, Michael J, PILZ, Daniela T, LAZAROU, Lazarus, COOPER, David N, SAMPSON, Julian R, BUTLER, Rachel, WHATLEY, Sharon D, CLARKE, Angus J, COLLEY, James P, RAVN, Kirstine, NIELSEN, Jytte Bieber, KERR, Alison, WILLIAMS, Elizabeth, CHRISTODOULOU, John, GECZ, Jozef, JARDINE, Philip E
Published in European journal of human genetics : EJHG (01.10.2005)
Published in European journal of human genetics : EJHG (01.10.2005)
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Journal Article
p.R270X MECP2 mutation and mortality in Rett syndrome
LE JIAN, ARCHER, Hayley L, RAVINE, David, KERR, Alison, DE KLERK, Nick, CHRISTODOULOU, John, BAILEY, Mark E. S, LAURVICK, Crystal, LEONARD, Helen
Published in European journal of human genetics : EJHG (01.11.2005)
Published in European journal of human genetics : EJHG (01.11.2005)
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Journal Article
NTNG1 mutations are a rare cause of Rett syndrome
Archer, Hayley L., Evans, Julie C., Millar, David S., Thompson, Peter W., Kerr, Alison M., Leonard, Helen, Christodoulou, John, Ravine, David, Lazarou, Lazarus, Grove, Lucy, Verity, Christopher, Whatley, Sharon D., Pilz, Daniela T., Sampson, Julian R., Clarke, Angus J.
Published in American journal of medical genetics. Part A (01.04.2006)
Published in American journal of medical genetics. Part A (01.04.2006)
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Journal Article