Brown J - Search Results

1

Monozygotic twins discordant for Ullrich-Turner syndrome.

Kaplowitz PB, Bodurtha J, Brown J, Spence JE. Kaplowitz PB, et al. Among authors: brown j. Am J Med Genet. 1991 Oct 1;41(1):78-82. doi: 10.1002/ajmg.1320410120. Am J Med Genet. 1991. PMID: 1951467

2

Partial trisomy 19p: case report and natural history.

Salbert BA, Solomon M, Spence JE, Jackson-Cook C, Brown J, Bodurtha J. Salbert BA, et al. Among authors: brown j. Clin Genet. 1992 Mar;41(3):143-6. doi: 10.1111/j.1399-0004.1992.tb03651.x. Clin Genet. 1992. PMID: 1563088

3

Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.

Cole H, Huang B, Salbert BA, Brown J, Howard-Peebles PN, Black SH, Dorfmann A, Febles OR, Stevens CA, Jackson-Cook C. Cole H, et al. Among authors: brown j. Am J Med Genet. 1994 Aug 15;52(2):136-45. doi: 10.1002/ajmg.1320520204. Am J Med Genet. 1994. PMID: 7801998 Review.

4

A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.

Goodship J, Curtis A, Cross I, Brown J, Emslie J, Wolstenholme J, Bhattacharya S, Burn J. Goodship J, et al. Among authors: brown j. J Med Genet. 1992 Jul;29(7):451-4. J Med Genet. 1992. PMID: 1640422 Free PMC article.

5

Blepharophimosis sequence and diaphragmatic hernia associated with interstitial deletion of chromosome 3 (46,XY,del(3)(q21q23)).

Wolstenholme J, Brown J, Masters KG, Wright C, English CJ. Wolstenholme J, et al. Among authors: brown j. J Med Genet. 1994 Aug;31(8):647-8. doi: 10.1136/jmg.31.8.647. J Med Genet. 1994. PMID: 7815425 Free PMC article.

6

Convalescent plasma in patients admitted to hospital with COVID-19 (RECOVERY): a randomised controlled, open-label, platform trial.

RECOVERY Collaborative Group. RECOVERY Collaborative Group. Lancet. 2021 May 29;397(10289):2049-2059. doi: 10.1016/S0140-6736(21)00897-7. Epub 2021 May 14. Lancet. 2021. PMID: 34000257 Free PMC article. Clinical Trial.

7

A prospective cytogenetic study of 36 cases of DiGeorge syndrome.

Wilson DI, Cross IE, Goodship JA, Brown J, Scambler PJ, Bain HH, Taylor JF, Walsh K, Bankier A, Burn J, et al. Wilson DI, et al. Among authors: brown j. Am J Hum Genet. 1992 Nov;51(5):957-63. Am J Hum Genet. 1992. PMID: 1415264 Free PMC article.

8

102T/C polymorphism of serotonin receptor type 2A gene is not associated with schizophrenia in either Chinese or British populations.

He L, Li T, Melville C, Liu S, Feng GY, Gu NF, Fox H, Shaw D, Breen G, Liu X, Sham P, Brown J, Collier D, St Clair D. He L, et al. Among authors: brown j. Am J Med Genet. 1999 Feb 5;88(1):95-8. Am J Med Genet. 1999. PMID: 10050975

9

Novel transcribed sequences neighbouring a translocation breakpoint associated with schizophrenia.

Devon RS, Evans KL, Maule JC, Christie S, Anderson S, Brown J, Shibasaki Y, Porteous DJ, Brookes AJ. Devon RS, et al. Among authors: brown j. Am J Med Genet. 1997 Feb 21;74(1):82-90. doi: 10.1002/(sici)1096-8628(19970221)74:1<82::aid-ajmg17>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9034012

10

An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.

Cross I, Delhanty J, Chapman P, Bowles LV, Griffin D, Wolstenholme J, Bradburn M, Brown J, Wood C, Gunn A, et al. Cross I, et al. Among authors: brown j. J Med Genet. 1992 Mar;29(3):175-9. doi: 10.1136/jmg.29.3.175. J Med Genet. 1992. PMID: 1313112 Free PMC article.

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