Francannet C - Search Results

1

Prenatal detection of mosaic isochromosome 20q: a fourth report with abnormal phenotype.

Goumy C, Beaufrère AM, Francannet C, Tchirkov A, Laurichesse Delmas H, Geissler F, Lemery D, Dechelotte PJ, Vago P. Goumy C, et al. Among authors: francannet c. Prenat Diagn. 2005 Aug;25(8):653-5. doi: 10.1002/pd.1216. Prenat Diagn. 2005. PMID: 16049989

2

Fraser syndrome with renal agenesis in two consanguineous Turkish families.

Francannet C, Lefrançois P, Dechelotte P, Robert E, Malpuech G, Robert JM. Francannet C, et al. Am J Med Genet. 1990 Aug;36(4):477-9. doi: 10.1002/ajmg.1320360421. Am J Med Genet. 1990. PMID: 2389805

3

[Value of muscle studies in the early diagnosis of Schwartz-Jampel syndrome].

Vanlieferighen P, Francannet C, Dechelotte P, Malpuech G, de Laguillaumie B, Storme B. Vanlieferighen P, et al. Among authors: francannet c. J Genet Hum. 1987 Aug;35(4):243-9. J Genet Hum. 1987. PMID: 3655749 French.

4

LADD syndrome in five members of a three-generation family and prenatal diagnosis.

Francannet C, Vanlieferinghen P, Dechelotte P, Urbain MF, Campagne D, Malpuech G. Francannet C, et al. Genet Couns. 1994;5(1):85-91. Genet Couns. 1994. PMID: 8031542 Review.

5

X-linked myopathy with excessive autophagy: a clinicopathological study of five new families.

Chabrol B, Figarella-Branger D, Coquet M, Mancini J, Fontan D, Pedespan JM, Francannet C, Pouget J, Beaufrère AM, Pellissier JF. Chabrol B, et al. Among authors: francannet c. Neuromuscul Disord. 2001 May;11(4):376-88. doi: 10.1016/s0960-8966(00)00209-1. Neuromuscul Disord. 2001. PMID: 11369189

6

Antenatal detection and impact on outcome of congenital diaphragmatic hernia: a 12-year experience in Auvergne, France.

Gallot D, Coste K, Francannet C, Laurichesse H, Boda C, Ughetto S, Vanlieferinghen P, Scheye T, Vendittelli F, Labbe A, Dechelotte PJ, Sapin V, Lemery D. Gallot D, et al. Among authors: francannet c. Eur J Obstet Gynecol Reprod Biol. 2006 Apr 1;125(2):202-5. doi: 10.1016/j.ejogrb.2005.06.030. Epub 2005 Aug 15. Eur J Obstet Gynecol Reprod Biol. 2006. PMID: 16099579

7

An unusual familial chromosome 9 "variant" with variable phenotype: characterization by CGH analysis.

Goumy C, Mihaescu M, Tchirkov A, Giollant M, Bonnet-Dupeyron MN, Jaffray JY, Geneix A, Perissel B, Francannet C, Boespflug-Tanguy O, Vago P. Goumy C, et al. Among authors: francannet c. Morphologie. 2005 Jun;89(285):71-5. doi: 10.1016/s1286-0115(05)83241-2. Morphologie. 2005. PMID: 16110742

8

De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.

Goumy C, Mihaescu M, Tchirkov A, Giollant M, Benier C, Francannet C, Jaffray JY, Geneix A, Vago P. Goumy C, et al. Among authors: francannet c. Genet Couns. 2006;17(3):371-9. Genet Couns. 2006. PMID: 17100206

9

Prenatal detection and outcome of congenital diaphragmatic hernia: a French registry-based study.

Gallot D, Boda C, Ughetto S, Perthus I, Robert-Gnansia E, Francannet C, Laurichesse-Delmas H, Jani J, Coste K, Deprest J, Labbe A, Sapin V, Lemery D. Gallot D, et al. Among authors: francannet c. Ultrasound Obstet Gynecol. 2007 Mar;29(3):276-83. doi: 10.1002/uog.3863. Ultrasound Obstet Gynecol. 2007. PMID: 17177265 Free article.

10

Trisomy 20q caused by interstitial duplication 20q13.2: clinical report and literature review.

Blanc P, Gouas L, Francannet C, Giollant M, Vago P, Goumy C. Blanc P, et al. Among authors: francannet c. Am J Med Genet A. 2008 May 15;146A(10):1307-11. doi: 10.1002/ajmg.a.32278. Am J Med Genet A. 2008. PMID: 18384146 Review.

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