Castel Y - Search Results

1

[A case of complete triploidy (69,XXY) in a premature infant. Presence of a clinical syndrome characteristic of this chromosome abnormality].

Castel Y, Rivière D, Toudic L, Alix D, Leroy JP. Castel Y, et al. Ann Pediatr (Paris). 1976 Oct 2;23(10):639-45. Ann Pediatr (Paris). 1976. PMID: 16106892 French. No abstract available.

2

[Congenital adenomatoid and cystic malformation of the lung. Anatomic and clinical presentation and discussion of 2 cases].

Volant A, Leroy JP, Alix D, Briere J, Balouet G, Castel Y. Volant A, et al. Among authors: castel y. Ann Pediatr (Paris). 1984 Oct;31(8):685-90. Ann Pediatr (Paris). 1984. PMID: 6497262 French. No abstract available.

3

[XXXXY syndrome].

Toudic L, L'Henoret G, Rivière D, L'Hour M, Castel Y. Toudic L, et al. Among authors: castel y. Arch Fr Pediatr. 1982 Apr;39(4):247-9. Arch Fr Pediatr. 1982. PMID: 7125819 French.

4

[Thanatophoric dwarfism. A anatomo-clinical case].

Toudic L, Leroy JP, Cozic A, Goude H, Castel Y. Toudic L, et al. Among authors: castel y. Ann Pediatr (Paris). 1976 Oct 2;23(10):633-7. Ann Pediatr (Paris). 1976. PMID: 16106891 Review. French. No abstract available.

5

[Two cases of cyclopia].

Castel Y, Riviere D, Toudic L, Nouaille Y, L'Henoret J, Duparcmeur H, Leroy JP, Balouet G. Castel Y, et al. Ann Pediatr (Paris). 1976 Oct 2;23(10):647-51. Ann Pediatr (Paris). 1976. PMID: 16106893 Review. French. No abstract available.

6

[Intra uterine major dwarfism with dysmorphia and severe encephalopathy. Bird head dwarfism (Virchow-Seckel type)].

Toudic L, Roche J, Alix D, Le Bars C, Dantoine G, Castel Y. Toudic L, et al. Among authors: castel y. Ann Pediatr (Paris). 1977 Oct;24(10):653-6. Ann Pediatr (Paris). 1977. PMID: 16211901 French. No abstract available.

7

[Apropos of a familial case of adrenoleukodystrophy related to X chromosome diagnosed prenatally].

Parent P, Le Meur F, Alix D, Le Fur JM, Toudic L, Castel Y. Parent P, et al. Among authors: castel y. Pediatrie. 1987;42(4):297-301. Pediatrie. 1987. PMID: 3671029 French.

8

[A new case of partial monosomy of chromosome 12,del(12)(p11.01 to p12.109) confirming the location of the gene for lactate dehydrogenase B].

Boilly-Dartigalongue B, Rivière D, Junien C, Couturier J, Toudic L, Marie F, Castel Y. Boilly-Dartigalongue B, et al. Among authors: castel y. Ann Genet. 1985;28(1):55-7. Ann Genet. 1985. PMID: 3874590 French.

9

[Association of trisomy 21 and gonosomal trisomy. Apropos of 2 cases].

Castel Y, Le Marec B, Toudic L, Lemarchand M, Cosson JP. Castel Y, et al. Pediatrie. 1983 Jun;38(4):235-41. Pediatrie. 1983. PMID: 6225989 French.

10

[Heterogeneity of Seckel syndrome? Apropos of a case].

Toudic L, Maroteaux P, Castel Y, Gouedard H, Parent P. Toudic L, et al. Among authors: castel y. Ann Pediatr (Paris). 1983 Nov;30(9):700-4. Ann Pediatr (Paris). 1983. PMID: 6660802 French. No abstract available.

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