Caille B - Search Results

1

Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness.

Bahuau M, Vidaud D, Kujas M, Palangié A, Assouline B, Chaignaud-Lebreton M, Prieur M, Vidaud M, Harpey JP, Lafourcade J, Caille B. Bahuau M, et al. Among authors: caille b. Ann Genet. 1997;40(2):78-91. Ann Genet. 1997. PMID: 9259954

2

Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors.

Bahuau M, Vidaud D, Jenkins RB, Bièche I, Kimmel DW, Assouline B, Smith JS, Alderete B, Cayuela JM, Harpey JP, Caille B, Vidaud M. Bahuau M, et al. Among authors: caille b. Cancer Res. 1998 Jun 1;58(11):2298-303. Cancer Res. 1998. PMID: 9622062

3

[A case report on a familial incidence of tumors].

Caille B, Lafourcade J. Caille B, et al. J Genet Hum. 1983 Mar;31(1):13-4. J Genet Hum. 1983. PMID: 6619805 French. No abstract available.

4

[Hypotonia and motor retardation in the infant. Use of electromyography and work-up strategy].

Renault F, Caille B, Harpey JP. Renault F, et al. Among authors: caille b. Ann Pediatr (Paris). 1992 Dec;39(10):611-3. Ann Pediatr (Paris). 1992. PMID: 1485774 French. No abstract available.

5

[Free 21 trisomy in mother and daughter].

Rethoré MO, Lafourcade J, Prieur M, Caille B, Cruveillier CJ, Tanzy M, Lejeune J. Rethoré MO, et al. Among authors: caille b. Ann Genet. 1970 Mar;13(1):42-5. Ann Genet. 1970. PMID: 5310104 French. No abstract available.

6

[Primary fibroelastosis of the endocardium. Genetic advice].

Roy C, Duriez S, Prieur M, Harpey JP, Lacroix J, Caille B, Cruveiller J, Lafourcade J. Roy C, et al. Among authors: caille b. Ann Pediatr (Paris). 1977 Dec;24(12):855-61. Ann Pediatr (Paris). 1977. PMID: 16218267 French. No abstract available.

7

[Longitudinal study of growth in Marfan's syndrome in early childhood].

Roy C, Renault F, Gourmelen M, Harpey JP, Caille B. Roy C, et al. Among authors: caille b. Ann Pediatr (Paris). 1983 Nov;30(9):665-70. Ann Pediatr (Paris). 1983. PMID: 6660800 French. No abstract available.

8

[Pseudohypoaldosteronism: familial forms. Eight case-reports, with a review of the literature (author's transl)].

Roy C, Cruveiller J, Harpey JP, Renault F, Debray P, Caille B. Roy C, et al. Among authors: caille b. Ann Pediatr (Paris). 1981 Oct;28(8):553-8. Ann Pediatr (Paris). 1981. PMID: 7305233 French. No abstract available.

9

[Neonatal hypotonias with congenital disproportion of various types of muscular fiber, especially type I fibers. Demonstration of the familial character of this new entity].

Fardeau M, Harpey JP, Caille B, Lafourcade J. Fardeau M, et al. Among authors: caille b. Arch Fr Pediatr. 1975 Dec;32(10):901-13. Arch Fr Pediatr. 1975. PMID: 1231675 French.

10

[Deletion of the short arm of chromosome 18, holoprosencephaly and pitressin-sensitive diabetes insipidus].

Noseda J, Valdes L, Caille B, Roy C, Harpey JP. Noseda J, et al. Among authors: caille b. Ann Pediatr (Paris). 1985 May;32(5):447-50. Ann Pediatr (Paris). 1985. PMID: 4026140 French. No abstract available.

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