Maltby EL[au] - Search Results

Year	Number of Results
1964	1
1984	1
1986	2
1987	2
1988	1
1992	1
1993	1
1995	1
1996	1
1997	1
1998	1
1999	1
2001	2
2004	1
2005	1
2010	1
2024	0

1

A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalities.

Elliott J, Maltby EL, Reynolds B. Elliott J, et al. Among authors: maltby el. J Med Genet. 1993 Mar;30(3):251-2. doi: 10.1136/jmg.30.3.251. J Med Genet. 1993. PMID: 7682620 Free PMC article. Review.

2

Duplication involving band 4q32 with minimal clinical effect.

Maltby EL, Barnes IC, Bennett CP. Maltby EL, et al. Am J Med Genet. 1999 Apr 23;83(5):431. doi: 10.1002/(sici)1096-8628(19990423)83:5<431::aid-ajmg20>3.0.co;2-k. Am J Med Genet. 1999. PMID: 10232760 No abstract available.

3

Folate sensitive site at 10q23 and its expression as a deletion.

Maltby EL, Higgins S. Maltby EL, et al. J Med Genet. 1987 May;24(5):299. doi: 10.1136/jmg.24.5.299. J Med Genet. 1987. PMID: 3585944 Free PMC article.

4

Baller Gerold syndrome and Fanconi anaemia.

Quarrell OW, Maltby EL, Harrison CJ. Quarrell OW, et al. Among authors: maltby el. Am J Med Genet. 1998 Jan 13;75(2):228-9. doi: 10.1002/(sici)1096-8628(19980113)75:2<228::aid-ajmg25>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9450894 No abstract available.

5

Xp21 muscular dystrophy due to X chromosome inversion.

Baxter PS, Maltby EL, Quarrell O. Baxter PS, et al. Among authors: maltby el. Neurology. 1997 Jul;49(1):260. doi: 10.1212/wnl.49.1.260. Neurology. 1997. PMID: 9222202

6

An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality.

Shannon NL, Maltby EL, Rigby AS, Quarrell OW. Shannon NL, et al. Among authors: maltby el. J Med Genet. 2001 Oct;38(10):674-9. doi: 10.1136/jmg.38.10.674. J Med Genet. 2001. PMID: 11584045 Free PMC article.

7

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein.

Sarafidou T, Kahl C, Martinez-Garay I, Mangelsdorf M, Gesk S, Baker E, Kokkinaki M, Talley P, Maltby EL, French L, Harder L, Hinzmann B, Nobile C, Richkind K, Finnis M, Deloukas P, Sutherland GR, Kutsche K, Moschonas NK, Siebert R, Gécz J; European Collaborative Consortium for the Study of ADLTE. Sarafidou T, et al. Among authors: maltby el. Genomics. 2004 Jul;84(1):69-81. doi: 10.1016/j.ygeno.2003.12.017. Genomics. 2004. PMID: 15203205

8

Prometaphase chromosome analysis as a routine diagnostic technique.

Barnes IC, Maltby EL. Barnes IC, et al. Among authors: maltby el. Clin Genet. 1986 May;29(5):378-83. doi: 10.1111/j.1399-0004.1986.tb00508.x. Clin Genet. 1986. PMID: 3742844

9

Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: Clinical assessment.

Barnicoat AJ, Bonneau JL, Boyd E, Docherty Z, Fennell SJ, Huret JL, King M, Maltby EL, McManus S, Pilz DT, Shafei-Benaissa E, Super M, Tolmie J. Barnicoat AJ, et al. Among authors: maltby el. Clin Genet. 1996 Jan;49(1):20-7. doi: 10.1111/j.1399-0004.1996.tb04319.x. Clin Genet. 1996. PMID: 8721567

10

Elevated p53 expression in benign meningiomas protects against recurrence and may be indicative of senescence.

Hakin-Smith V, Battersby RD, Maltby EL, Timperley WR, Royds JA. Hakin-Smith V, et al. Among authors: maltby el. Neuropathol Appl Neurobiol. 2001 Feb;27(1):40-9. doi: 10.1046/j.0305-1846.2001.00300.x. Neuropathol Appl Neurobiol. 2001. PMID: 11299001 Clinical Trial.

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