Sarda P - Search Results

1

Interstitial deletion of the distal long arm of chromosome 4.

Sarda P, Lefort G, Fryns JP, Humeau C, Rieu D. Sarda P, et al. J Med Genet. 1992 Apr;29(4):259-61. doi: 10.1136/jmg.29.4.259. J Med Genet. 1992. PMID: 1583648 Free PMC article.

2

Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.

Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F. Lefort G, et al. Among authors: sarda p. Am J Med Genet. 2002 Dec 15;113(4):333-8. doi: 10.1002/ajmg.b.10720. Am J Med Genet. 2002. Corrected and republished in: Am J Med Genet A. 2003 Apr 15;118A(2):333-8. PMID: 12457404 Corrected and republished.

3

Interstitial deletion of chromosome 1 del (1) (q32 q42): case report and review of the literature.

Sarda P, Lefort G, Taviaux S, Humeau C, Rieu D. Sarda P, et al. Clin Genet. 1992 Jan;41(1):25-7. doi: 10.1111/j.1399-0004.1992.tb03623.x. Clin Genet. 1992. PMID: 1633642 Review.

4

Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.

Sarda P, Lefort G, Devaux P, Humeau C, Rieu D. Sarda P, et al. Ann Genet. 1992;35(2):117-20. Ann Genet. 1992. PMID: 1524409

5

Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.

Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F. Lefort G, et al. Among authors: sarda p. Am J Med Genet A. 2003 Apr 15;118A(2):333-8. Am J Med Genet A. 2003. PMID: 12698965

6

Duplication 8q12: confirmation of a novel recognizable phenotype with duane retraction syndrome and developmental delay.

Amouroux C, Vincent M, Blanchet P, Puechberty J, Schneider A, Chaze AM, Girard M, Tournaire M, Jorgensen C, Morin D, Sarda P, Lefort G, Geneviève D. Amouroux C, et al. Among authors: sarda p. Eur J Hum Genet. 2012 May;20(5):580-3. doi: 10.1038/ejhg.2011.243. Epub 2012 Jan 18. Eur J Hum Genet. 2012. PMID: 22258531 Free PMC article.

7

Epidemiology of diaphragmatic hernia in Languedoc-Roussillon.

Sarda P, Devaux P, Lefort G, Humeau C, Rieu D. Sarda P, et al. Genet Couns. 1991;2(2):77-81. Genet Couns. 1991. PMID: 1781958

8

[F.G. syndrome: a rare and/or extremely polymorphic syndrome?].

Sarda P, Lefort G, Jalaguier J, Bonnet H. Sarda P, et al. J Genet Hum. 1989 Dec;37(4-5):401-3. J Genet Hum. 1989. PMID: 2635717 French.

9

Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.

Blanchet P, Lefort G, Eglin MC, Rieu D, Sarda P. Blanchet P, et al. Among authors: sarda p. Genet Couns. 1993;4(4):289-94. Genet Couns. 1993. PMID: 8110417

10

X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French family.

Lefort G, Taib J, Toutain A, Houdayer C, Moraine CI, Humeau C, Sarda P. Lefort G, et al. Among authors: sarda p. Ann Genet. 1993;36(4):200-5. Ann Genet. 1993. PMID: 8166424

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