Dunnill MG - Search Results

1

The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.

van Steensel M, Smith FJ, Steijlen PM, Kluijt I, Stevens HP, Messenger A, Kremer H, Dunnill MG, Kennedy C, Munro CS, Doherty VR, McGrath JA, Covello SP, Coleman CM, Uitto J, McLean WH. van Steensel M, et al. Among authors: dunnill mg. Am J Hum Genet. 1999 Aug;65(2):413-9. doi: 10.1086/302506. Am J Hum Genet. 1999. PMID: 10417283 Free PMC article.

2

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa.

Kivirikko S, McGrath JA, Baudoin C, Aberdam D, Ciatti S, Dunnill MG, McMillan JR, Eady RA, Ortonne JP, Meneguzzi G, et al. Kivirikko S, et al. Among authors: dunnill mg. Hum Mol Genet. 1995 May;4(5):959-62. doi: 10.1093/hmg/4.5.959. Hum Mol Genet. 1995. PMID: 7633458

3

Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition.

McGrath JA, Gatalica B, Li K, Dunnill MG, McMillan JR, Christiano AM, Eady RA, Uitto J. McGrath JA, et al. Among authors: dunnill mg. Am J Pathol. 1996 Jun;148(6):1787-96. Am J Pathol. 1996. PMID: 8669466 Free PMC article.

4

First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus sampling.

McGrath JA, Dunnill MG, Christiano AM, Lake BD, Atherton DJ, Rodeck CH, Pope FM, Eady RA, Uitto J. McGrath JA, et al. Among authors: dunnill mg. Br J Dermatol. 1996 Apr;134(4):734-9. doi: 10.1111/j.1365-2133.1996.tb06981.x. Br J Dermatol. 1996. PMID: 8733382

5

A recurrent laminin 5 mutation in British patients with lethal (Herlitz) junctional epidermolysis bullosa: evidence for a mutational hotspot rather than propagation of an ancestral allele.

Ashton GH, Mellerio JE, Dunnill MG, Pulkkinen L, Christiano AM, Uitto J, Eady RA, McGrath JA. Ashton GH, et al. Among authors: dunnill mg. Br J Dermatol. 1997 May;136(5):674-7. Br J Dermatol. 1997. PMID: 9205497

6

Recurrent mutations in the type VII collagen gene (COL7A1) in patients with recessive dystrophic epidermolysis bullosa.

Mellerio JE, Dunnill MG, Allison W, Ashton GH, Christiano AM, Uitto J, Eady RA, McGrath JA. Mellerio JE, et al. Among authors: dunnill mg. J Invest Dermatol. 1997 Aug;109(2):246-9. doi: 10.1111/1523-1747.ep12319792. J Invest Dermatol. 1997. PMID: 9242516 Free article.

7

Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: implications for prenatal diagnosis in one family.

McGrath JA, McMillan JR, Dunnill MG, Pulkkinen L, Christiano AM, Rodeck CH, Eady RA, Uitto J. McGrath JA, et al. Among authors: dunnill mg. Prenat Diagn. 1995 Jul;15(7):647-54. doi: 10.1002/pd.1970150710. Prenat Diagn. 1995. PMID: 8532625

8

Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosa.

Dunnill MG, McGrath JA, Richards AJ, Christiano AM, Uitto J, Pope FM, Eady RA. Dunnill MG, et al. J Invest Dermatol. 1996 Aug;107(2):171-7. doi: 10.1111/1523-1747.ep12329570. J Invest Dermatol. 1996. PMID: 8757758 Free article.

9

Recurrent molecular abnormalities in type VII collagen in Southern Italian patients with recessive dystrophic epidermolysis bullosa.

Ashton GH, Mellerio JE, Dunnill MG, Milana G, Mayou BJ, Carrera J, McGrath JA, Eady RA. Ashton GH, et al. Among authors: dunnill mg. Clin Exp Dermatol. 1999 May;24(3):232-5. doi: 10.1046/j.1365-2230.1999.00461.x. Clin Exp Dermatol. 1999. PMID: 10354186

10

Twice-daily vs. once-daily inpatient dithranol for psoriasis.

Kirkup ME, Sabroe RA, Kavanagh GM, Downs AM, Sansom JE, de Berker DA, Dunnill MG, Kennedy CT, Archer CB. Kirkup ME, et al. Among authors: dunnill mg. Clin Exp Dermatol. 2002 Nov;27(8):695-9. doi: 10.1046/j.1365-2230.2002.01106.x. Clin Exp Dermatol. 2002. PMID: 12472549 Clinical Trial.

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