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124 results
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[Renal agenesis and the Fraser syndrome: 4 observations].
Vanlieferinghen P, Francannet C, Robert E, Malpuech G, Robert JM. Vanlieferinghen P, et al. Among authors: francannet c. J Genet Hum. 1989 Dec;37(4-5):373-7. J Genet Hum. 1989. PMID: 2635714 French.
Immunopathological manifestations in Kabuki syndrome: a registry study of 177 individuals.
Margot H, Boursier G, Duflos C, Sanchez E, Amiel J, Andrau JC, Arpin S, Brischoux-Boucher E, Boute O, Burglen L, Caille C, Capri Y, Collignon P, Conrad S, Cormier-Daire V, Delplancq G, Dieterich K, Dollfus H, Fradin M, Faivre L, Fernandes H, Francannet C, Gatinois V, Gerard M, Goldenberg A, Ghoumid J, Grotto S, Guerrot AM, Guichet A, Isidor B, Jacquemont ML, Julia S, Khau Van Kien P, Legendre M, Le Quan Sang KH, Leheup B, Lyonnet S, Magry V, Manouvrier S, Martin D, Morel G, Munnich A, Naudion S, Odent S, Perrin L, Petit F, Philip N, Rio M, Robbe J, Rossi M, Sarrazin E, Toutain A, Van Gils J, Vera G, Verloes A, Weber S, Whalen S, Sanlaville D, Lacombe D, Aladjidi N, Geneviève D. Margot H, et al. Among authors: francannet c. Genet Med. 2020 Jan;22(1):181-188. doi: 10.1038/s41436-019-0623-x. Epub 2019 Jul 31. Genet Med. 2020. PMID: 31363182 Free article.
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
[Diagnosis of deficiency in cofactor of phenylalanine hydroxylase: a metabolic emergency].
Meyer M, Malpuech G, Geneste J, Palcoux JB, Francannet C, Vanlieferinghen P. Meyer M, et al. Among authors: francannet c. J Genet Hum. 1989 Dec;37(4-5):315-9. J Genet Hum. 1989. PMID: 2517561 French.
[Congenital stenosis of the aqueduct of Sylvius transmitted in an autosomal recessive mode (5 cases in 2 families)].
Vanlieferinghen P, Chazal J, Francannet C, Malpuech G, Storme B. Vanlieferinghen P, et al. Among authors: francannet c. J Genet Hum. 1987 Aug;35(4):251-8. J Genet Hum. 1987. PMID: 3498797 French.
[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.
[Contribution of anatomic verification of the fetus and newborn infant in diagnosis and genetic counseling. Apropos of 221 autopsies].
Dechelotte P, Malpuech G, Jacquetin B, Francannet C, Vanlieferinghen P, Charbonne F, De Laguillaumie B. Dechelotte P, et al. Among authors: francannet c. J Genet Hum. 1985 Sep;33(3-4):283-8. J Genet Hum. 1985. PMID: 4056751 French.
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.
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
[Macrocephaly-capillary malformation. A neonatal case].
Coste K, Sarret C, Cisse A, Delabaere A, Francannet C, Vanlieferinghen P. Coste K, et al. Among authors: francannet c. Arch Pediatr. 2012 Sep;19(9):917-20. doi: 10.1016/j.arcped.2012.06.017. Epub 2012 Aug 9. Arch Pediatr. 2012. PMID: 22884750 French.
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