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Items: 26

1.

Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?

White M, Conroy J, Bullman H, Lever M, Daly E, Betts DR, Cody D, Crolla JA, Lynch SA.

Case Rep Genet. 2013;2013:764152. doi: 10.1155/2013/764152. Epub 2013 Jan 14.

2.

Pseudohypoparathyroidism type 1b due to paternal uniparental disomy of chromosome 20q.

Dixit A, Chandler KE, Lever M, Poole RL, Bullman H, Mughal MZ, Steggall M, Suri M.

J Clin Endocrinol Metab. 2013 Jan;98(1):E103-8. doi: 10.1210/jc.2012-2639. Epub 2012 Nov 8. Review.

PMID:
23144470
3.

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci.

Turner CL, Mackay DM, Callaway JL, Docherty LE, Poole RL, Bullman H, Lever M, Castle BM, Kivuva EC, Turnpenny PD, Mehta SG, Mansour S, Wakeling EL, Mathew V, Madden J, Davies JH, Temple IK.

Eur J Hum Genet. 2010 Jun;18(6):648-55. doi: 10.1038/ejhg.2009.246. Epub 2010 Jan 27.

4.

Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14.

Temple IK, Shrubb V, Lever M, Bullman H, Mackay DJ.

BMJ Case Rep. 2009;2009. pii: bcr06.2009.1997. doi: 10.1136/bcr.06.2009.1997. Epub 2009 Jul 1.

5.

Coincidence of a novel KCNJ11 missense variant R365H with a paternally inherited 6q24 duplication in a patient with transient neonatal diabetes.

Staník J, Lethby M, Flanagan SE, Gasperíková D, Milosovicová B, Lever M, Bullman H, Zubcevic L, Hattersley AT, Ellard S, Ashcroft FM, Klimes I.

Diabetes Care. 2008 Sep;31(9):1736-7. doi: 10.2337/dc08-0549. Epub 2008 Jun 12.

6.

Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.

Bullman H, Lever M, Robinson DO, Mackay DJ, Holder SE, Wakeling EL.

J Med Genet. 2008 Jun;45(6):396-9. doi: 10.1136/jmg.2007.057059. Epub 2008 May 12.

PMID:
18474587
7.

Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14.

Temple IK, Shrubb V, Lever M, Bullman H, Mackay DJ.

J Med Genet. 2007 Oct;44(10):637-40. Epub 2007 Jun 29.

8.

Parental mosaic trisomy 21 detected following maternal cell contamination of an amniotic fluid specimen from a normal male pregnancy.

Street ML, Barber JC, Boyle TA, Ellis KH, Bullman H, Homfray T.

Prenat Diagn. 2007 Sep;27(9):858-60.

PMID:
17554802
10.

Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome.

Joyce CA, Sharp A, Walker JM, Bullman H, Temple IK.

Hum Genet. 1999 Sep;105(3):273-80.

PMID:
10987657
11.

Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.

Eccles DM, van der Luijt R, Breukel C, Bullman H, Bunyan D, Fisher A, Barber J, du Boulay C, Primrose J, Burn J, Fodde R.

Am J Hum Genet. 1996 Dec;59(6):1193-201.

12.

Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophy.

Bunyan DJ, Robinson DO, Collins AL, Cockwell AE, Bullman HM, Whittaker PA.

Hum Genet. 1994 May;93(5):541-4.

PMID:
8168831
13.

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation.

Macpherson JN, Bullman H, Youings SA, Jacobs PA.

Hum Mol Genet. 1994 Mar;3(3):399-405.

PMID:
8012351
14.

Population studies of the fragile X: a molecular approach.

Jacobs PA, Bullman H, Macpherson J, Youings S, Rooney V, Watson A, Dennis NR.

J Med Genet. 1993 Jun;30(6):454-9.

15.

Physical characterization of the replication origin of the cryptic plasmid pCB101 isolated from Clostridium butyricum NCIB 7423.

Brehm JK, Pennock A, Bullman HM, Young M, Oultram JD, Minton NP.

Plasmid. 1992 Jul;28(1):1-13.

PMID:
1518909
16.

Nucleotide sequence of the Erwinia chrysanthemi NCPPB 1066 L-asparaginase gene.

Minton NP, Bullman HM, Scawen MD, Atkinson T, Gilbert HJ.

Gene. 1986;46(1):25-35.

PMID:
3026924
17.

Cloning and expression of the Erwinia chrysanthemi asparaginase gene in Escherichia coli and Erwinia carotovora.

Gilbert HJ, Blazek R, Bullman HM, Minton NP.

J Gen Microbiol. 1986 Jan;132(1):151-60.

PMID:
3011958
18.

Organization and evolution of the class I gene family in the major histocompatibility complex of the C57BL/10 mouse.

Weiss EH, Golden L, Fahrner K, Mellor AL, Devlin JJ, Bullman H, Tiddens H, Bud H, Flavell RA.

Nature. 1984 Aug 23-29;310(5979):650-5.

PMID:
6088985
19.

Molecular cloning and analysis of H-2 class I genes of H-2b haplotype mice.

Mellor AL, Golden L, Weiss E, Bullman H, Bud H, Flavell RA.

Transplant Proc. 1983 Dec;15(4):2013-5. No abstract available.

PMID:
6424287
20.

Structure and expression of the human globin genes and murine histocompatibility antigen genes.

Flavell RA, Grosveld F, Busslinger M, de Boer E, Kioussis D, Mellor AL, Golden L, Weiss E, Hurst J, Bud H, Bullman H, Simpson E, James R, Townsend AR, Taylor PM, Schmidt W, Ferluga J, Leben L, Santamaria M, Atfield G, Festenstein H.

Cold Spring Harb Symp Quant Biol. 1983;47 Pt 2:1067-78. No abstract available.

PMID:
6305573
21.

Expression of murine H-2Kb histocompatibility antigen in cells transformed with cloned H-2 genes.

Mellor AL, Golden L, Weiss E, Bullman H, Hurst J, Simpson E, James RF, Townsend AR, Taylor PM, Schmidt W, Ferluga J, Leben L, Santamaria M, Atfield G, Festenstein H, Flavell RA.

Nature. 1982 Aug 5;298(5874):529-34.

PMID:
6285197
22.

The structure and expression of mammalian gene clusters.

Flavell RA, Bud H, Bullman H, Busslinger M, deBoer E, deKleine A, Golden L, Groffen J, Grosveld FG, Mellor AL, Moschonas N, Weiss E.

Prog Clin Biol Res. 1982;103 Pt A:37-55. No abstract available.

PMID:
6298806
23.

High-pressure liquid chromatography of steroids secreted by human adrenal and testis cells in monolayer culture.

O'Hare MJ, Nice EC, Magee-Brown R, Bullman H.

J Chromatogr. 1976 Sep 29;125(1):357-67.

PMID:
977682
24.
26.

Carcinoembryonic antigens of erythrocyte membranes.

Nery R, Bullman H, Barsoum AL.

Nat New Biol. 1973 Nov 14;246(150):44-6. No abstract available.

PMID:
4128113

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