Seller M - Search Results

1

Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

Mangiarini L, Sathasivam K, Mahal A, Mott R, Seller M, Bates GP. Mangiarini L, et al. Among authors: seller m. Nat Genet. 1997 Feb;15(2):197-200. doi: 10.1038/ng0297-197. Nat Genet. 1997. PMID: 9020849

2

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice.

Mangiarini L, Sathasivam K, Seller M, Cozens B, Harper A, Hetherington C, Lawton M, Trottier Y, Lehrach H, Davies SW, Bates GP. Mangiarini L, et al. Among authors: seller m. Cell. 1996 Nov 1;87(3):493-506. doi: 10.1016/s0092-8674(00)81369-0. Cell. 1996. PMID: 8898202 Free article.

3

Linkage studies in dominant optic atrophy, Kjer type: possible evidence for heterogeneity.

Seller MJ, Behnam JT, Lewis CM, Johnston RL, Burdon MA, Spalton DJ. Seller MJ, et al. J Med Genet. 1997 Dec;34(12):967-72. doi: 10.1136/jmg.34.12.967. J Med Genet. 1997. PMID: 9429135 Free PMC article.

4

A 45,X/69,XXY fetus.

Betts DR, Fear CN, Barby T, Seller MJ. Betts DR, et al. Among authors: seller mj. Clin Genet. 1989 Apr;35(4):285-8. doi: 10.1111/j.1399-0004.1989.tb02945.x. Clin Genet. 1989. PMID: 2714016

5

A fetus with an X;1 balanced reciprocal translocation and eye disease.

Seller MJ, Pal K, Horsley S, Davies AF, Berry AC, Meredith R, McCartney AC. Seller MJ, et al. J Med Genet. 1995 Jul;32(7):557-60. doi: 10.1136/jmg.32.7.557. J Med Genet. 1995. PMID: 7562972 Free PMC article.

6

Further evidence for an intermittent pattern of neural tube closure in humans.

Seller MJ. Seller MJ. J Med Genet. 1995 Mar;32(3):205-7. doi: 10.1136/jmg.32.3.205. J Med Genet. 1995. PMID: 7783170 Free PMC article.

7

Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique.

Mackie-Ogilvie C, Waddle K, Mandeville J, Seller MJ, Docherty Z. Mackie-Ogilvie C, et al. Among authors: seller mj. J Med Genet. 1997 Nov;34(11):912-6. doi: 10.1136/jmg.34.11.912. J Med Genet. 1997. PMID: 9391885 Free PMC article.

8

Trisomy 15 mosaicism in an IVF fetus.

Bennett CP, Davis T, Seller MJ. Bennett CP, et al. Among authors: seller mj. J Med Genet. 1992 Oct;29(10):745-6. doi: 10.1136/jmg.29.10.745. J Med Genet. 1992. PMID: 1433239 Free PMC article.

9

Pseudotrisomy 13 and autosomal recessive holoprosencephaly.

Seller MJ, Chitty LS, Dunbar H. Seller MJ, et al. J Med Genet. 1993 Nov;30(11):970-1. doi: 10.1136/jmg.30.11.970. J Med Genet. 1993. PMID: 8301659 Free PMC article.

10

Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities.

Bennett CP, Betts DR, Seller MJ. Bennett CP, et al. Among authors: seller mj. J Med Genet. 1991 Apr;28(4):280-1. doi: 10.1136/jmg.28.4.280. J Med Genet. 1991. PMID: 1856837 Free PMC article.

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