Simpson NE - Search Results

1

Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

Mulligan LM, Phillips MA, Forster-Gibson CJ, Beckett J, Partington MW, Simpson NE, Holden JJ, White BN. Mulligan LM, et al. Among authors: simpson ne. Am J Hum Genet. 1985 May;37(3):463-72. Am J Hum Genet. 1985. PMID: 2988332 Free PMC article.

2

Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.

Goodfellow PJ, White BN, Holden JJ, Duncan AM, Sears EV, Wang HS, Berlin L, Kidd KK, Simpson NE. Goodfellow PJ, et al. Among authors: simpson ne. Am J Hum Genet. 1985 Sep;37(5):890-7. Am J Hum Genet. 1985. PMID: 2864854 Free PMC article.

3

An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.

Farrer LA, Goodfellow PJ, Lamarche CM, Franjkovic I, Myers S, White BN, Holden JJ, Kidd JR, Simpson NE, Kidd KK. Farrer LA, et al. Among authors: simpson ne. Am J Hum Genet. 1987 Apr;40(4):329-37. Am J Hum Genet. 1987. PMID: 2883889 Free PMC article.

4

An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis.

Forster-Gibson CJ, Mulligan LM, Simpson NE, White BN, Holden JJ. Forster-Gibson CJ, et al. Among authors: simpson ne. Am J Med Genet. 1986 Jan-Feb;23(1-2):665-83. doi: 10.1002/ajmg.1320230159. Am J Med Genet. 1986. PMID: 3006491

5

The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications.

Forster-Gibson CJ, Mulligan LM, Partington MW, Simpson NE, Holden JJ, White BN. Forster-Gibson CJ, et al. Among authors: simpson ne. J Neurogenet. 1985 Jun;2(3):231-7. doi: 10.3109/01677068509100152. J Neurogenet. 1985. PMID: 3860635

6

Fragile-X syndrome III: dermatoglyphic studies in males.

Simpson NE, Newman BJ, Partington MW. Simpson NE, et al. Am J Med Genet. 1984 Jan;17(1):195-207. doi: 10.1002/ajmg.1320170112. Am J Med Genet. 1984. PMID: 6711595

7

Localization and linkage of three polymorphic DNA sequences on human chromosome 20.

Goodfellow PJ, Duncan AM, Farrer LA, Holden JJ, White BN, Kidd JR, Kidd KK, Simpson NE. Goodfellow PJ, et al. Among authors: simpson ne. Cytogenet Cell Genet. 1987;44(2-3):112-7. doi: 10.1159/000132354. Cytogenet Cell Genet. 1987. PMID: 2882953

8

Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against synteny.

Farrer LA, Goodfellow PJ, White BN, Holden JJ, Kidd JR, Simpson NE, Kidd KK. Farrer LA, et al. Among authors: simpson ne. Cancer Genet Cytogenet. 1987 Aug;27(2):327-34. doi: 10.1016/0165-4608(87)90015-x. Cancer Genet Cytogenet. 1987. PMID: 2885081

9

Regional localization of 18 human X-linked DNA sequences.

Riddell DC, Wang HS, Beckett J, Chan A, Holden JJ, Mulligan LM, Phillips MA, Simpson NE, Wrogemann K, Hamerton JL, et al. Riddell DC, et al. Among authors: simpson ne. Cytogenet Cell Genet. 1986;42(3):123-8. doi: 10.1159/000132264. Cytogenet Cell Genet. 1986. PMID: 3460742

10

Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13.

Beckett J, Holden JJ, Simpson NE, White BN, MacLeod PM. Beckett J, et al. Among authors: simpson ne. J Neurogenet. 1986 Jul;3(4):225-31. doi: 10.3109/01677068609106852. J Neurogenet. 1986. PMID: 3462379

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