Gosden CM - Search Results

1

Identifying genes within microdissected genomic DNA: isolation of brain expressed genes from a translocation region associated with inherited mental illness.

Brookes AJ, Slorach EM, Evans KL, Thomson ML, Gosden CM, Muir WJ, Porteous DJ. Brookes AJ, et al. Among authors: gosden cm. Mamm Genome. 1995 Apr;6(4):257-62. doi: 10.1007/BF00352412. Mamm Genome. 1995. PMID: 7613030

2

Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia.

Muir WJ, Gosden CM, Brookes AJ, Fantes J, Evans KL, Maguire SM, Stevenson B, Boyle S, Blackwood DH, St Clair DM, et al. Muir WJ, et al. Among authors: gosden cm. Cytogenet Cell Genet. 1995;70(1-2):35-40. doi: 10.1159/000133986. Cytogenet Cell Genet. 1995. PMID: 7736785

3

Association within a family of a balanced autosomal translocation with major mental illness.

St Clair D, Blackwood D, Muir W, Carothers A, Walker M, Spowart G, Gosden C, Evans HJ. St Clair D, et al. Lancet. 1990 Jul 7;336(8706):13-6. doi: 10.1016/0140-6736(90)91520-k. Lancet. 1990. PMID: 1973210

4

Seeding of YACs over regions 1q41-q42.3 and 11q14.3-q23 with microdissection clones.

Petit J, Boisseau P, Evans K, Christie S, Gosden C, Muir W, St Clair D, Porteous D, Arveiler B. Petit J, et al. Eur J Hum Genet. 1995;3(6):351-6. doi: 10.1159/000472324. Eur J Hum Genet. 1995. PMID: 8825577

5

The candidate Wilms' tumour gene is involved in genitourinary development.

Pritchard-Jones K, Fleming S, Davidson D, Bickmore W, Porteous D, Gosden C, Bard J, Buckler A, Pelletier J, Housman D, et al. Pritchard-Jones K, et al. Nature. 1990 Jul 12;346(6280):194-7. doi: 10.1038/346194a0. Nature. 1990. PMID: 2164159

6

Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness.

Sharp CW, Muir WJ, Blackwood DH, Walker M, Gosden C, St Clair DM. Sharp CW, et al. Am J Med Genet. 1994 Dec 15;54(4):354-60. doi: 10.1002/ajmg.1320540414. Am J Med Genet. 1994. PMID: 7726208

7

De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.

Bonthron DT, Smith SJ, Fantes J, Gosden CM. Bonthron DT, et al. Among authors: gosden cm. Am J Hum Genet. 1993 Sep;53(3):629-37. Am J Hum Genet. 1993. PMID: 8352273 Free PMC article.

8

Parental origin of transcription from the human GNAS1 gene.

Campbell R, Gosden CM, Bonthron DT. Campbell R, et al. Among authors: gosden cm. J Med Genet. 1994 Aug;31(8):607-14. doi: 10.1136/jmg.31.8.607. J Med Genet. 1994. PMID: 7815417 Free PMC article.

9

Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation.

Strain L, Porteous ME, Gosden CM, Ellis PM, Neilson JP, Bonthron DT. Strain L, et al. Among authors: gosden cm. Prenat Diagn. 1994 Jun;14(6):469-74. doi: 10.1002/pd.1970140610. Prenat Diagn. 1994. PMID: 7937584

10

Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.

Strain L, Gosden CM, Brock DJ, Bonthron DT. Strain L, et al. Among authors: gosden cm. Am J Hum Genet. 1994 Feb;54(2):236-43. Am J Hum Genet. 1994. PMID: 8304340 Free PMC article.

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