Mortimer PS - Search Results

1

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

Jones GE, Ostergaard P, Moore AT, Connell FC, Williams D, Quarrell O, Brady AF, Spier I, Hazan F, Moldovan O, Wieczorek D, Mikat B, Petit F, Coubes C, Saul RA, Brice G, Gordon K, Jeffery S, Mortimer PS, Vasudevan PC, Mansour S. Jones GE, et al. Among authors: mortimer ps. Eur J Hum Genet. 2014 Jul;22(7):881-7. doi: 10.1038/ejhg.2013.263. Epub 2013 Nov 27. Eur J Hum Genet. 2014. PMID: 24281367 Free PMC article.

2

Managing lymphoedema.

Mortimer PS. Mortimer PS. Clin Exp Dermatol. 1995 Mar;20(2):98-106. doi: 10.1111/j.1365-2230.1995.tb02665.x. Clin Exp Dermatol. 1995. PMID: 8565266 Review.

3

Mapping of primary congenital lymphedema to the 5q35.3 region.

Evans AL, Brice G, Sotirova V, Mortimer P, Beninson J, Burnand K, Rosbotham J, Child A, Sarfarazi M. Evans AL, et al. Am J Hum Genet. 1999 Feb;64(2):547-55. doi: 10.1086/302248. Am J Hum Genet. 1999. PMID: 9973292 Free PMC article.

4

A gene for lymphedema-distichiasis maps to 16q24.3.

Mangion J, Rahman N, Mansour S, Brice G, Rosbotham J, Child AH, Murday VA, Mortimer PS, Barfoot R, Sigurdsson A, Edkins S, Sarfarazi M, Burnand K, Evans AL, Nunan TO, Stratton MR, Jeffery S. Mangion J, et al. Among authors: mortimer ps. Am J Hum Genet. 1999 Aug;65(2):427-32. doi: 10.1086/302500. Am J Hum Genet. 1999. PMID: 10417285 Free PMC article.

5

Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphy.

Rosbotham JL, Brice GW, Child AH, Nunan TO, Mortimer PS, Burnand KG. Rosbotham JL, et al. Among authors: mortimer ps. Br J Dermatol. 2000 Jan;142(1):148-52. doi: 10.1046/j.1365-2133.2000.03258.x. Br J Dermatol. 2000. PMID: 10651712

6

Reduction of the genetic interval for lyphoedema-distichiasis to below 2 Mb.

Bell R, Brice G, Child AH, Murday VA, Mansour S, Sandy CJ, Collin JR, Mortimer P, Callen DF, Burnand K. Bell R, et al. J Med Genet. 2000 Sep;37(9):725. doi: 10.1136/jmg.37.9.725. J Med Genet. 2000. PMID: 11182939 Free PMC article. No abstract available.

7

Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene.

Bell R, Brice G, Child AH, Murday VA, Mansour S, Sandy CJ, Collin JR, Brady AF, Callen DF, Burnand K, Mortimer P, Jeffery S. Bell R, et al. Hum Genet. 2001 Jun;108(6):546-51. doi: 10.1007/s004390100528. Hum Genet. 2001. PMID: 11499682

8

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.

Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF, Sarfarazi M, Burnand KG, Jeffery S, Mortimer P, Murday VA. Brice G, et al. J Med Genet. 2002 Jul;39(7):478-83. doi: 10.1136/jmg.39.7.478. J Med Genet. 2002. PMID: 12114478 Free PMC article.

9

Clinicopathological case 2: lymphoedema-distichiasis syndrome.

Ameen M, Brice G, Mortimer PS. Ameen M, et al. Among authors: mortimer ps. Clin Exp Dermatol. 2003 Jul;28(4):463-4. doi: 10.1046/j.1365-2230.2003.01277.x. Clin Exp Dermatol. 2003. PMID: 12823324 No abstract available.

10

Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema.

Evans AL, Bell R, Brice G, Comeglio P, Lipede C, Jeffery S, Mortimer P, Sarfarazi M, Child AH. Evans AL, et al. J Med Genet. 2003 Sep;40(9):697-703. doi: 10.1136/jmg.40.9.697. J Med Genet. 2003. PMID: 12960217 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

261 results

Search Page

Filters