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Items: 13

1.

Behaviour changes in an adult with Down syndrome.

Forster-Gibson CJ.

Can Fam Physician. 2019 Apr;65(Suppl 1):S25-S26. No abstract available.

2.

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders.

Liu X, Novosedlik N, Wang A, Hudson ML, Cohen IL, Chudley AE, Forster-Gibson CJ, Lewis SM, Holden JJ.

Eur J Hum Genet. 2009 Feb;17(2):228-35. doi: 10.1038/ejhg.2008.148. Epub 2008 Aug 27.

3.

Cryptic duplication of 21q in an individual with a clinical diagnosis of Down syndrome.

Forster-Gibson CJ, Davies J, MacKenzie JJ, Harrison K.

Clin Genet. 2001 Jun;59(6):438-43.

PMID:
11453976
4.

Multiple endocrine neoplasia type 2.

Forster-Gibson CJ, Mulligan LM.

Eur J Cancer. 1994;30A(13):1969-74. Review. No abstract available.

PMID:
7734209
6.

A linkage study of primary affective disorder.

Waters B, Sengar D, Marchenko I, Rock G, Lapierre Y, Forster-Gibson CJ, Simpson NE.

Br J Psychiatry. 1988 Apr;152:560-2.

PMID:
3167412
7.

Linkage studies of Friedreich ataxia by means of blood-group and protein markers.

Keats BJ, Ward LJ, Lu M, Krieger S, Wilensky MA, Forster-Gibson CJ, Roy M, Monté M, Barbeau A, Simpson NE, et al.

Am J Hum Genet. 1987 Oct;41(4):627-34.

8.

A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h].

Wrogemann K, Arveiler B, Oberle I, Mulligan LM, Holden JA, Forster-Gibson CJ, White BN.

Nucleic Acids Res. 1986 Jul 11;14(13):5572. No abstract available.

9.

Machado-Joseph disease: linkage analysis between the loci for the disease and 18 protein markers.

Myers SM, MacLeod PM, Forse RA, Forster-Gibson CJ, Simpson NE.

Cytogenet Cell Genet. 1986;43(3-4):226-8. No abstract available.

PMID:
3467903
10.

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.

Am J Med Genet. 1986 Jan-Feb;23(1-2):665-83.

PMID:
3006491
11.

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.

J Neurogenet. 1985 Jun;2(3):231-7.

PMID:
3860635
12.

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.

Am J Hum Genet. 1985 May;37(3):463-72.

13.

Temperature-dependent cytosol-to-nucleus translocation of the Ah receptor for 2,3,7,8-tetrachlorodibenzo-p-dioxin in continuous cell culture lines.

Okey AB, Bondy GP, Mason ME, Nebert DW, Forster-Gibson CJ, Muncan J, Dufresne MJ.

J Biol Chem. 1980 Dec 10;255(23):11415-22. No abstract available.

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