Pritchard MA - Search Results

1

The interleukin-4 receptor gene (IL4R) maps to 16p11.2-16p12.1 in human and to the distal region of mouse chromosome 7.

Pritchard MA, Baker E, Whitmore SA, Sutherland GR, Idzerda RL, Park LS, Cosman D, Jenkins NA, Gilbert DJ, Copeland NG, et al. Pritchard MA, et al. Genomics. 1991 Jul;10(3):801-6. doi: 10.1016/0888-7543(91)90466-r. Genomics. 1991. PMID: 1679753

2

Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24.

Pritchard MA, Baker E, Callen DF, Sutherland GR, Wilks AF. Pritchard MA, et al. Mamm Genome. 1992;3(1):36-8. doi: 10.1007/BF00355839. Mamm Genome. 1992. PMID: 1581631

3

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.

Kremer EJ, Pritchard M, Lynch M, Yu S, Holman K, Baker E, Warren ST, Schlessinger D, Sutherland GR, Richards RI. Kremer EJ, et al. Science. 1991 Jun 21;252(5013):1711-4. doi: 10.1126/science.1675488. Science. 1991. PMID: 1675488

4

Localization of the human GM-CSF receptor gene to the X-Y pseudoautosomal region.

Gough NM, Gearing DP, Nicola NA, Baker E, Pritchard M, Callen DF, Sutherland GR. Gough NM, et al. Nature. 1990 Jun 21;345(6277):734-6. doi: 10.1038/345734a0. Nature. 1990. PMID: 1972780

5

Hereditary unstable DNA: a new explanation for some old genetic questions?

Sutherland GR, Haan EA, Kremer E, Lynch M, Pritchard M, Yu S, Richards RI. Sutherland GR, et al. Lancet. 1991 Aug 3;338(8762):289-92. doi: 10.1016/0140-6736(91)90426-p. Lancet. 1991. PMID: 1677119

6

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.

Richards RI, Holman K, Kozman H, Kremer E, Lynch M, Pritchard M, Yu S, Mulley J, Sutherland GR. Richards RI, et al. J Med Genet. 1991 Dec;28(12):818-23. doi: 10.1136/jmg.28.12.818. J Med Genet. 1991. PMID: 1757956 Free PMC article.

7

Fragile X genotype characterized by an unstable region of DNA.

Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D, et al. Yu S, et al. Science. 1991 May 24;252(5009):1179-81. doi: 10.1126/science.252.5009.1179. Science. 1991. PMID: 2031189

8

Molecular cloning and chromosomal localisation of the human homologue of a receptor related to tyrosine kinases (RYK).

Stacker SA, Hovens CM, Vitali A, Pritchard MA, Baker E, Sutherland GR, Wilks AF. Stacker SA, et al. Among authors: pritchard ma. Oncogene. 1993 May;8(5):1347-56. Oncogene. 1993. PMID: 8386829

9

Isolation of a human DNA sequence which spans the fragile X.

Kremer EJ, Yu S, Pritchard M, Nagaraja R, Heitz D, Lynch M, Baker E, Hyland VJ, Little RD, Wada M, et al. Kremer EJ, et al. Am J Hum Genet. 1991 Sep;49(3):656-61. Am J Hum Genet. 1991. PMID: 1882843 Free PMC article.

10

Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence.

Sutherland GR, Gedeon A, Kornman L, Donnelly A, Byard RW, Mulley JC, Kremer E, Lynch M, Pritchard M, Yu S, et al. Sutherland GR, et al. N Engl J Med. 1991 Dec 12;325(24):1720-2. doi: 10.1056/NEJM199112123252407. N Engl J Med. 1991. PMID: 1944473 Free article. No abstract available.

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