Lowther GW - Search Results

1

Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency.

Bennett MJ, Allison F, Lowther GW, Gray RG, Johnston DI, Fitzsimmons JS, Manning NJ, Pollitt RJ. Bennett MJ, et al. Among authors: lowther gw. Prenat Diagn. 1987 Feb;7(2):135-41. doi: 10.1002/pd.1970070210. Prenat Diagn. 1987. PMID: 3575262

2

A case of 2-methylacetoacetyl CoA thiolase deficiency with coincidental chromosome abnormalities.

Gray RG, Lowther GW, Littlewood JM, Middleton B, Bennett MJ. Gray RG, et al. Among authors: lowther gw. J Med Genet. 1984 Oct;21(5):397. doi: 10.1136/jmg.21.5.397. J Med Genet. 1984. PMID: 6150117 Free PMC article. No abstract available.

3

Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies.

Morris A, Boyd E, Dhanjal S, Lowther GW, Aitken DA, Young J, Menzies AL, Imrie SJ, Connor JM. Morris A, et al. Among authors: lowther gw. Prenat Diagn. 1999 Jun;19(6):546-51. Prenat Diagn. 1999. PMID: 10416971 Clinical Trial.

4

The predictive value of findings of the common aneuploidies, trisomies 13, 18 and 21, and numerical sex chromosome abnormalities at CVS: experience from the ACC U.K. Collaborative Study. Association of Clinical Cytogeneticists Prenatal Diagnosis Working Party.

Smith K, Lowther G, Maher E, Hourihan T, Wilkinson T, Wolstenholme J. Smith K, et al. Prenat Diagn. 1999 Sep;19(9):817-26. Prenat Diagn. 1999. PMID: 10521838 Clinical Trial.

5

Midtrimester chorionic villus sampling: an alternative approach?

Cameron AD, Murphy KW, McNay MB, Mathers AM, Kingdom J, Aitken DA, Crossley J, Imrie S, Lowther G. Cameron AD, et al. Am J Obstet Gynecol. 1994 Oct;171(4):1035-7. doi: 10.1016/0002-9378(94)90029-9. Am J Obstet Gynecol. 1994. PMID: 7943067 Clinical Trial.

6

Second-trimester placental biopsy for rapid fetal karyotyping.

Cameron AD, Mathers AM, Wisdom S, Johnstone J, MacKenzie JR, Walker JJ, Imrie SJ, Lowther GW, Connor JM. Cameron AD, et al. Among authors: lowther gw. Am J Obstet Gynecol. 1990 Sep;163(3):931-4. doi: 10.1016/0002-9378(90)91099-x. Am J Obstet Gynecol. 1990. PMID: 2403171

7

Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings.

Carothers AD, Boyd E, Lowther G, Ellis PM, Couzin DA, Faed MJ, Robb A. Carothers AD, et al. Genet Epidemiol. 1999;16(2):179-90. doi: 10.1002/(SICI)1098-2272(1999)16:2<179::AID-GEPI5>3.0.CO;2-7. Genet Epidemiol. 1999. PMID: 10030400

8

Prenatal diagnosis in the United Kingdom--an overview.

Lowther GW, Whittle MJ. Lowther GW, et al. Eur J Hum Genet. 1997;5 Suppl 1:84-9. Eur J Hum Genet. 1997. PMID: 9101186 Review.

9

Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease.

Whiteford ML, Coutts J, al-Roomi L, Mather A, Lowther G, Cooke A, Vaughan JI, Moore GE, Tolmie JL. Whiteford ML, et al. Prenat Diagn. 1995 Jun;15(6):579-84. doi: 10.1002/pd.1970150613. Prenat Diagn. 1995. PMID: 7659692

10

Congenital ocular defects associated with an abnormality of the human chromosome 1: trisomy 1q32-qter.

Clark BJ, Lowther GW, Lee WR. Clark BJ, et al. Among authors: lowther gw. J Pediatr Ophthalmol Strabismus. 1994 Jan-Feb;31(1):41-5. doi: 10.3928/0191-3913-19940101-09. J Pediatr Ophthalmol Strabismus. 1994. PMID: 8195962

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