Gosden C - Search Results

1

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. Among authors: gosden c. Am J Med Genet. 1994 Dec 15;54(4):354-60. doi: 10.1002/ajmg.1320540414. Am J Med Genet. 1994. PMID: 7726208

2

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. Among authors: gosden c. Lancet. 1990 Jul 7;336(8706):13-6. doi: 10.1016/0140-6736(90)91520-k. Lancet. 1990. PMID: 1973210

3

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

4

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

5

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. Among authors: gosden c. Eur J Hum Genet. 1995;3(6):351-6. doi: 10.1159/000472324. Eur J Hum Genet. 1995. PMID: 8825577

6

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.

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

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.

9

Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.

Little MH, Williamson KA, Mannens M, Kelsey A, Gosden C, Hastie ND, van Heyningen V. Little MH, et al. Among authors: gosden c. Hum Mol Genet. 1993 Mar;2(3):259-64. doi: 10.1093/hmg/2.3.259. Hum Mol Genet. 1993. PMID: 8388765

10

Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture.

McKinley MJ, Kearney LU, Nicolaides KH, Gosden CM, Webb TP, Fryns JP. McKinley MJ, et al. Among authors: gosden cm. Am J Med Genet. 1988 May-Jun;30(1-2):355-68. doi: 10.1002/ajmg.1320300136. Am J Med Genet. 1988. PMID: 3177458

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