Fraser NA - Search Results

1

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.

Gal A, Schinzel A, Orth U, Fraser NA, Mollica F, Craig IW, Kruse T, Mächler M, Neugebauer M, Bleeker-Wagemakers LM. Gal A, et al. Among authors: fraser na. Hum Genet. 1989 Mar;81(4):315-8. doi: 10.1007/BF00283682. Hum Genet. 1989. PMID: 2564836

2

Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.

Sefiani A, Sinnett D, Abel L, Szpiro-Tapia S, Heuertz S, Craig I, Fraser N, Kruse TA, Frydman M, Peter MO, et al. Sefiani A, et al. Hum Genet. 1988 Nov;80(3):282-6. doi: 10.1007/BF01790098. Hum Genet. 1988. PMID: 3192215

3

Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27 beta (DXS255).

Meitinger T, Fraser NA, Lorenz B, Zrenner E, Murken J, Craig IW. Meitinger T, et al. Among authors: fraser na. Hum Genet. 1989 Feb;81(3):283-6. doi: 10.1007/BF00279005. Hum Genet. 1989. PMID: 2921039

4

Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq.

Ballabio A, Carrozzo R, Gil A, Gillard B, Affara N, Ferguson-Smith MA, Fraser N, Craig I, Rocchi M, Romeo G. Ballabio A, et al. Ann Hum Genet. 1989 Jan;53(1):9-14. doi: 10.1111/j.1469-1809.1989.tb01117.x. Ann Hum Genet. 1989. PMID: 2729897

5

Localisation of Y chromosome sequences in normal and 'XX' males.

Buckle VJ, Boyd Y, Fraser N, Goodfellow PN, Goodfellow PJ, Wolfe J, Craig IW. Buckle VJ, et al. J Med Genet. 1987 Apr;24(4):197-203. doi: 10.1136/jmg.24.4.197. J Med Genet. 1987. PMID: 3035183 Free PMC article.

6

Detecting maternal cell contamination in prenatal diagnosis.

Craig I, Ross M, Edwards JH, Fraser N, Hall J. Craig I, et al. Lancet. 1989 May 13;1(8646):1074-5. doi: 10.1016/s0140-6736(89)92468-9. Lancet. 1989. PMID: 2566019 No abstract available.

7

The mammalian Y chromosome: molecular search for the sex-determining gene--summary and perspectives.

Craig I, Levy E, Fraser N. Craig I, et al. Development. 1987;101 Suppl:185-90. Development. 1987. PMID: 3503718

8

Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene?

Fraser N, Ballabio A, Zollo M, Persico G, Craig I. Fraser N, et al. Development. 1987;101 Suppl:127-32. doi: 10.1242/dev.101.Supplement.127. Development. 1987. PMID: 3503710

9

Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.

Ballabio A, Parenti G, Carrozzo R, Sebastio G, Andria G, Buckle V, Fraser N, Craig I, Rocchi M, Romeo G, et al. Ballabio A, et al. Proc Natl Acad Sci U S A. 1987 Jul;84(13):4519-23. doi: 10.1073/pnas.84.13.4519. Proc Natl Acad Sci U S A. 1987. PMID: 3474618 Free PMC article.

10

X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: application of the probe M27 beta to evaluate X inactivation status.

Schmidt M, Du Sart D, Kalitsis P, Fraser N, Leversha M, Voullaire L, Foster D, Davies J, Hills L, Petrovic V, et al. Schmidt M, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):411-5. doi: 10.1002/ajmg.1320380252. Am J Med Genet. 1991. PMID: 1673316

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