Lunt P - Search Results

1

Implementing genetic education in primary care: the Gen-Equip programme.

Paneque M, Cornel MC, Curtisova V, Houwink E, Jackson L, Kent A, Lunt P, Macek M, Stefansdottir V, Turchetti D, Skirton H. Paneque M, et al. Among authors: lunt p. J Community Genet. 2017 Apr;8(2):147-150. doi: 10.1007/s12687-017-0296-6. Epub 2017 Mar 13. J Community Genet. 2017. PMID: 28289980 Free PMC article.

2

The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages.

Jackson L, O'Connor A, Paneque M, Curtisova V, Lunt PW, Pourova RK, Macek M Jr, Stefansdottir V, Turchetti D, Campos M, Henneman L, Godino L, Skirton H, Cornel MC. Jackson L, et al. Genet Med. 2019 Mar;21(3):718-726. doi: 10.1038/s41436-018-0132-3. Epub 2018 Jul 27. Genet Med. 2019. PMID: 30050101 Free PMC article.

3

Correction: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages.

Jackson L, O'Connor A, Paneque M, Curtisova V, Lunt PW, Pourova RK, MacekJr M, Stefansdottir V, Turchetti D, Campos M, Henneman L, Godino L, Skirton H, Cornel MC. Jackson L, et al. Genet Med. 2019 Jul;21(7):1669. doi: 10.1038/s41436-018-0279-y. Genet Med. 2019. PMID: 30139992 Free PMC article.

4

A systematic review of interventions to provide genetics education for primary care.

Paneque M, Turchetti D, Jackson L, Lunt P, Houwink E, Skirton H. Paneque M, et al. Among authors: lunt p. BMC Fam Pract. 2016 Jul 22;17:89. doi: 10.1186/s12875-016-0483-2. BMC Fam Pract. 2016. PMID: 27445117 Free PMC article. Review.

5

A three generation family with fibrodysplasia ossificans progressiva.

Connor JM, Skirton H, Lunt PW. Connor JM, et al. Among authors: lunt pw. J Med Genet. 1993 Aug;30(8):687-9. doi: 10.1136/jmg.30.8.687. J Med Genet. 1993. PMID: 8411056 Free PMC article.

6

A new family linked to the RP1 dominant retinitis pigmentosa locus on chromosome 8q.

Inglehearn CF, McHale JC, Keen TJ, Skirton H, Lunt PW. Inglehearn CF, et al. Among authors: lunt pw. J Med Genet. 1999 Aug;36(8):646-8. J Med Genet. 1999. PMID: 10465120 Free PMC article. No abstract available.

7

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).

Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, Woollard WJ, Dafou D, Kilo T, Smithson S, Lunt P, Murday VA, Hodgson S, Keenan R, Pilz DT, Martinez-Corral I, Makinen T, Mortimer PS, Jeffery S, Trembath RC, Mansour S. Ostergaard P, et al. Among authors: lunt p. Nat Genet. 2011 Sep 4;43(10):929-31. doi: 10.1038/ng.923. Nat Genet. 2011. PMID: 21892158

8

Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis.

Jardine PE, Cotter PD, Johnson SA, Fitzsimons EJ, Tyfield L, Lunt PW, Bishop DF. Jardine PE, et al. Among authors: lunt pw. J Med Genet. 1994 Mar;31(3):213-8. doi: 10.1136/jmg.31.3.213. J Med Genet. 1994. PMID: 7912287 Free PMC article. Review.

9

A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.

Upadhyaya M, Lunt PW, Sarfarazi M, Broadhead W, Daniels J, Owen M, Harper PS. Upadhyaya M, et al. Among authors: lunt pw. J Med Genet. 1991 Oct;28(10):665-71. doi: 10.1136/jmg.28.10.665. J Med Genet. 1991. PMID: 1941963 Free PMC article.

10

Holoprosencephaly: a family showing dominant inheritance and variable expression.

Collins AL, Lunt PW, Garrett C, Dennis NR. Collins AL, et al. Among authors: lunt pw. J Med Genet. 1993 Jan;30(1):36-40. doi: 10.1136/jmg.30.1.36. J Med Genet. 1993. PMID: 8423605 Free PMC article.

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