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The Schinzel-Giedion syndrome.
al-Gazali LI, Farndon P, Burn J, Flannery DB, Davison C, Mueller RF. al-Gazali LI, et al. Among authors: farndon p. J Med Genet. 1990 Jan;27(1):42-7. doi: 10.1136/jmg.27.1.42. J Med Genet. 1990. PMID: 2407846 Free PMC article. Review. No abstract available.
Linkage data for Marfan syndrome and markers on chromosomes 1 and 11.
de Groote J, Farndon PA, Kilpatrick MV, de Paepe A, Oorthuys JW, Nevin NC, Child AH, Pope FM. de Groote J, et al. Among authors: farndon pa. J Med Genet. 1990 Feb;27(2):82-5. doi: 10.1136/jmg.27.2.82. J Med Genet. 1990. PMID: 1969489 Free PMC article.
Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disorders.
Schanze D, Harakalova M, Stevens CA, Brancati F, Dallapiccola B, Farndon P, Ferraz VE, McDonald-McGinn DM, Zackai EH, Wright M, van Lieshout S, Vogel MJ, van Haelst MM, Zenker M. Schanze D, et al. Among authors: farndon p. Am J Med Genet A. 2013 Dec;161A(12):3012-7. doi: 10.1002/ajmg.a.36119. Epub 2013 Sep 24. Am J Med Genet A. 2013. PMID: 24115501
The fetal valproate syndrome.
DiLiberti JH, Farndon PA, Dennis NR, Curry CJ. DiLiberti JH, et al. Among authors: farndon pa. Am J Med Genet. 1984 Nov;19(3):473-81. doi: 10.1002/ajmg.1320190308. Am J Med Genet. 1984. PMID: 6439041
A recombination map of the human X-chromosome.
Del Mastro RG, Farndon PA, Kilpatrick MW. Del Mastro RG, et al. Among authors: farndon pa. Hum Genet. 1990 Dec;86(2):228-30. doi: 10.1007/BF00197710. Hum Genet. 1990. PMID: 2265835
Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.
Marchegiani S, Davis T, Tessadori F, van Haaften G, Brancati F, Hoischen A, Huang H, Valkanas E, Pusey B, Schanze D, Venselaar H, Vulto-van Silfhout AT, Wolfe LA, Tifft CJ, Zerfas PM, Zambruno G, Kariminejad A, Sabbagh-Kermani F, Lee J, Tsokos MG, Lee CC, Ferraz V, da Silva EM, Stevens CA, Roche N, Bartsch O, Farndon P, Bermejo-Sanchez E, Brooks BP, Maduro V, Dallapiccola B, Ramos FJ, Chung HY, Le Caignec C, Martins F, Jacyk WK, Mazzanti L, Brunner HG, Bakkers J, Lin S, Malicdan MC, Boerkoel CF, Gahl WA, de Vries BB, van Haelst MM, Zenker M, Markello TC. Marchegiani S, et al. Among authors: farndon p. Am J Hum Genet. 2015 Jul 2;97(1):99-110. doi: 10.1016/j.ajhg.2015.05.017. Epub 2015 Jun 25. Am J Hum Genet. 2015. PMID: 26119818 Free PMC article.
An exclusion map of Marfan syndrome.
Blanton SH, Sarfarazi M, Eiberg H, de Groote J, Farndon PA, Kilpatrick MW, Child AH, Pope FM, Peltonen L, Francomano CA, et al. Blanton SH, et al. Among authors: farndon pa. J Med Genet. 1990 Feb;27(2):73-7. doi: 10.1136/jmg.27.2.73. J Med Genet. 1990. PMID: 2319588 Free PMC article.
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