Maltby EL - 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
2008	2
2010	1
2025	0

1

Maltby EL, Ironside JW, Battersby RD. Maltby EL, et al. Cancer Genet Cytogenet. 1988 Apr;31(2):199-210. doi: 10.1016/0165-4608(88)90218-x. Cancer Genet Cytogenet. 1988. PMID: 3162394

2

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.

3

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.

4

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.

5

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.

6

Molecular abnormalities in pediatric barrett esophagus: can we test for potential of neoplastic progression?

Maltby EL, Dyson MJ, Wheeler MR, Thomson M, Sethuraman C, Cohen MC. Maltby EL, et al. Pediatr Dev Pathol. 2010 Jul-Aug;13(4):310-7. doi: 10.2350/09-08-0700-OA.1. Pediatr Dev Pathol. 2010. PMID: 20053129

7

Familial pericentric inversion (13) detected by antenatal diagnosis.

Maltby EL. Maltby EL. J Med Genet. 1984 Apr;21(2):149-51. doi: 10.1136/jmg.21.2.149. J Med Genet. 1984. PMID: 6716417 Free PMC article.

8

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.

9

Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation.

Young ID, Zuccollo JM, Maltby EL, Broderick NJ. Young ID, et al. Among authors: maltby el. J Med Genet. 1992 Apr;29(4):251-2. doi: 10.1136/jmg.29.4.251. J Med Genet. 1992. PMID: 1583645 Free PMC article.

10

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

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