Craig IW - Search Results

1

Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2.

Tümer Z, Tommerup N, Tønnesen T, Kreuder J, Craig IW, Horn N. Tümer Z, et al. Among authors: craig iw. Hum Genet. 1992 Mar;88(6):668-72. doi: 10.1007/BF02265295. Hum Genet. 1992. PMID: 1348049

2

Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia.

Rack KA, Chelly J, Gibbons RJ, Rider S, Benjamin D, Lafreniére RG, Oscier D, Hendriks RW, Craig IW, Willard HF, et al. Rack KA, et al. Among authors: craig iw. Hum Mol Genet. 1994 Jul;3(7):1053-9. doi: 10.1093/hmg/3.7.1053. Hum Mol Genet. 1994. PMID: 7981672

3

A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome.

Bech-Hansen NT, Field LL, Schramm AM, Reedyk M, Craig IW, Fraser NJ, Pearce WG. Bech-Hansen NT, et al. Among authors: craig iw. Hum Genet. 1990 Apr;84(5):406-8. doi: 10.1007/BF00195809. Hum Genet. 1990. PMID: 1969841

4

Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS.

Notarangelo LD, Parolini O, Porta F, Locatelli F, Lanfranchi A, Marconi M, Nespoli L, Albertini A, Craig IW, Ugazio AG. Notarangelo LD, et al. Among authors: craig iw. Hum Genet. 1991 Dec;88(2):237-41. doi: 10.1007/BF00206081. Hum Genet. 1991. PMID: 1684569

5

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: craig iw. Hum Genet. 1989 Mar;81(4):315-8. doi: 10.1007/BF00283682. Hum Genet. 1989. PMID: 2564836

6

Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.

de Saint Basile G, Notarangelo LD, Bonaiti-Pellié C, Doussau M, Prolini O, Craig IW, Ugazio A, Griscelli C, Fischer A. de Saint Basile G, et al. Among authors: craig iw. Hum Genet. 1992 May;89(2):223-8. doi: 10.1007/BF00217127. Hum Genet. 1992. PMID: 1350264 Clinical Trial.

7

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene.

Hendriks RW, Chen ZY, Hinds H, Schuurman RK, Craig IW. Hendriks RW, et al. Among authors: craig iw. Hum Mol Genet. 1992 Jun;1(3):187-94. doi: 10.1093/hmg/1.3.187. Hum Mol Genet. 1992. PMID: 1303176

8

The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.

Sims KB, Lebo RV, Benson G, Shalish C, Schuback D, Chen ZY, Bruns G, Craig IW, Golbus MS, Breakefield XO. Sims KB, et al. Among authors: craig iw. Hum Mol Genet. 1992 May;1(2):83-9. doi: 10.1093/hmg/1.2.83. Hum Mol Genet. 1992. PMID: 1301161

9

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.

Coleman M, Bhattacharya S, Lindsay S, Wright A, Jay M, Litt M, Craig I, Davies K. Coleman M, et al. Am J Hum Genet. 1990 Dec;47(6):935-40. Am J Hum Genet. 1990. PMID: 2239970 Free PMC article.

10

Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes.

Craig IW, Mill J, Craig GM, Loat C, Schalkwyk LC. Craig IW, et al. Among authors: craig gm. Eur J Hum Genet. 2004 Aug;12(8):639-46. doi: 10.1038/sj.ejhg.5201212. Eur J Hum Genet. 2004. PMID: 15114374

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