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156 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: malpuech g. J Genet Hum. 1989 Dec;37(4-5):373-7. J Genet Hum. 1989. PMID: 2635714 French.
Pulmonary hyperplasia in Fraser syndrome.
Labbé A, Dechelotte P, Lemery D, Malpuech G. Labbé A, et al. Among authors: malpuech g. Pediatr Pulmonol. 1992 Oct;14(2):131-4. doi: 10.1002/ppul.1950140212. Pediatr Pulmonol. 1992. PMID: 1437351 No abstract available.
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. Among authors: malpuech g. Am J Med Genet. 1990 Aug;36(4):477-9. doi: 10.1002/ajmg.1320360421. Am J Med Genet. 1990. PMID: 2389805
[Outcome of the kidney with vesico-ureteral reflux. Apropos of 129 cases].
Martin P, Palcoux JB, Merle P, Vincens L, Malpuech G. Martin P, et al. Among authors: malpuech g. Pediatrie. 1989;44(8):665-9. Pediatrie. 1989. PMID: 2622708 French.
[Neuroblastoma in the Auvergne region from 1986 to 1991: epidemiological data].
Gembara P, Dechelotte P, Chazal J, Chauvin F, Chopard P, Goddon R, Goumy P, Masson A, Malpuech G, Deméocq F. Gembara P, et al. Among authors: malpuech g. Pediatrie. 1993;48(11):801-4. Pediatrie. 1993. PMID: 8058441 Review. 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. Among authors: malpuech g. Genet Couns. 1994;5(1):85-91. Genet Couns. 1994. PMID: 8031542 Review.
[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. 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: malpuech g. J Genet Hum. 1985 Sep;33(3-4):283-8. J Genet Hum. 1985. PMID: 4056751 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: malpuech g. J Genet Hum. 1987 Aug;35(4):243-9. J Genet Hum. 1987. PMID: 3655749 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: malpuech g. J Genet Hum. 1987 Aug;35(4):251-8. J Genet Hum. 1987. PMID: 3498797 French.
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