Flint J - Search Results

1

Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: an inherited encephalopathy of childhood?

Nokelainen P, Heiskala H, Raininko R, Autti T, Wirtavuori K, Häkkinen AM, Flint J. Nokelainen P, et al. Among authors: flint j. Am J Med Genet. 2001 Oct 15;103(3):198-206. doi: 10.1002/ajmg.1536.abs. Am J Med Genet. 2001. PMID: 11745991

2

Genetic effects on human cognition: lessons from the study of mental retardation syndromes.

Nokelainen P, Flint J. Nokelainen P, et al. Among authors: flint j. J Neurol Neurosurg Psychiatry. 2002 Mar;72(3):287-96. doi: 10.1136/jnnp.72.3.287. J Neurol Neurosurg Psychiatry. 2002. PMID: 11861682 Free PMC article. Review.

3

The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.

Flint J, Knight S. Flint J, et al. Curr Opin Genet Dev. 2003 Jun;13(3):310-6. doi: 10.1016/s0959-437x(03)00049-2. Curr Opin Genet Dev. 2003. PMID: 12787795

4

The genetics of mental retardation.

Flint J, Wilkie AO. Flint J, et al. Br Med Bull. 1996 Jul;52(3):453-64. doi: 10.1093/oxfordjournals.bmb.a011559. Br Med Bull. 1996. PMID: 8949249 Review.

5

Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis.

Knight SJ, Flint J. Knight SJ, et al. Among authors: flint j. J Med Genet. 2000 Jun;37(6):401-9. doi: 10.1136/jmg.37.6.401. J Med Genet. 2000. PMID: 10851249 Free PMC article. Review.

6

Clinical studies on submicroscopic subtelomeric rearrangements: a checklist.

de Vries BB, White SM, Knight SJ, Regan R, Homfray T, Young ID, Super M, McKeown C, Splitt M, Quarrell OW, Trainer AH, Niermeijer MF, Malcolm S, Flint J, Hurst JA, Winter RM. de Vries BB, et al. Among authors: flint j. J Med Genet. 2001 Mar;38(3):145-50. doi: 10.1136/jmg.38.3.145. J Med Genet. 2001. PMID: 11238680 Free PMC article.

7

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation.

Flint J, Wilkie AO, Buckle VJ, Winter RM, Holland AJ, McDermid HE. Flint J, et al. Nat Genet. 1995 Feb;9(2):132-40. doi: 10.1038/ng0295-132. Nat Genet. 1995. PMID: 7719339

8

Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13).

de Vries BB, Lees M, Knight SJ, Regan R, Corney D, Flint J, Barnicoat A, Winter RM. de Vries BB, et al. Among authors: flint j. Am J Med Genet. 2001 Apr 1;99(4):314-9. doi: 10.1002/ajmg.1182. Am J Med Genet. 2001. PMID: 11251999

9

Subtle chromosomal rearrangements in children with unexplained mental retardation.

Knight SJ, Regan R, Nicod A, Horsley SW, Kearney L, Homfray T, Winter RM, Bolton P, Flint J. Knight SJ, et al. Among authors: flint j. Lancet. 1999 Nov 13;354(9191):1676-81. doi: 10.1016/S0140-6736(99)03070-6. Lancet. 1999. PMID: 10568569

10

The genetic basis for mental retardation.

Raynham H, Gibbons R, Flint J, Higgs D. Raynham H, et al. Among authors: flint j. QJM. 1996 Mar;89(3):169-75. doi: 10.1093/qjmed/89.3.169. QJM. 1996. PMID: 8731560 Review. No abstract available.

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