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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. J Genet Hum. 1989 Dec;37(4-5):373-7. J Genet Hum. 1989. PMID: 2635714 French.
[Partial deletion 10qter. A new case].
Vanlieferinghen P, Dechelotte P, Charbonné F. Vanlieferinghen P, et al. Ann Genet. 1987;30(2):118-21. Ann Genet. 1987. PMID: 3314664 Review. French.
[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: vanlieferinghen p. J Genet Hum. 1989 Dec;37(4-5):315-9. J Genet Hum. 1989. PMID: 2517561 French.
[Prenatal diagnosis of X-linked adrenal hypoplasia associated with glycerol kinase deficiency].
Malpuech G, Dastugue B, Giraud G, Jouanel P, Vanlieferinghen P, Carla H. Malpuech G, et al. Among authors: vanlieferinghen p. J Genet Hum. 1989 Jun;37(2):155-62. J Genet Hum. 1989. PMID: 2545811 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: vanlieferinghen p. J Genet Hum. 1985 Sep;33(3-4):283-8. J Genet Hum. 1985. PMID: 4056751 French.
Johanson-Blizzard syndrome. a new case with autopsy findings.
Vanlieferinghen PH, Borderon C, Francannet CH, Gembara P, Dechelotte P. Vanlieferinghen PH, et al. Genet Couns. 2001;12(3):245-50. Genet Couns. 2001. PMID: 11693787 Review.
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. Among authors: vanlieferinghen p. Genet Couns. 1994;5(1):85-91. Genet Couns. 1994. PMID: 8031542 Review.
[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. J Genet Hum. 1987 Aug;35(4):251-8. J Genet Hum. 1987. PMID: 3498797 French.
[Evaluation of a three-year (1988-1990) prenatal screening of malformative uropathies in the department of Puy-de-Dôme].
Palcoux JB, Lemery D, Vanlieferinghen P, Desvignes V, Francannet P, Dechelotte P. Palcoux JB, et al. Among authors: vanlieferinghen p. Pediatrie. 1992;47(10):699-703. Pediatrie. 1992. PMID: 1337595 French.
[Macrocephaly-capillary malformation. A neonatal case].
Coste K, Sarret C, Cisse A, Delabaere A, Francannet C, Vanlieferinghen P. Coste K, et al. Among authors: vanlieferinghen p. 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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