Poissonnier M - Search Results

1

[Genetic counseling in a case of neuro-ectodermosis: Vera Price trichothiodystrophy. Brittle hair with reduced sulfur content].

Poissonnier M, Blanc A, Bat P. Poissonnier M, et al. J Genet Hum. 1988 Aug;36(4):361-5. J Genet Hum. 1988. PMID: 3221211 French. No abstract available.

2

Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases.

Poissonnier M, Turleau C, Olivier-Martin M, Milleret-Proyart MJ, Prieur M, Dubos M, Cabanis MO, Mugneret F, Blanc P, Noel L. Poissonnier M, et al. Ann Genet. 1992;35(3):146-51. Ann Genet. 1992. PMID: 1466563 Review.

3

[Familial primary myeloproliferative syndrome. Three cases in the same family].

Poissonnier M, Gruyer P, Noël L, Brière J, Tulliez M, Castaigne S. Poissonnier M, et al. J Genet Hum. 1988 Aug;36(4):367-71. J Genet Hum. 1988. PMID: 3221212 French. No abstract available.

4

[Fatal hypoplasia of the left heart in 2 brothers an reciprocal chromosome translocation (8;11) (p211;pl.53) in their mother: difficulties in genetic counseling].

Poissonnier M, Maroteaux-Chauvet ML, Aurias A, Couillard F. Poissonnier M, et al. J Genet Hum. 1981 Sep;29(3):297-319. J Genet Hum. 1981. PMID: 7334351 French. No abstract available.

5

[Familial cancer of the colon without polyposis and the familial cancer syndrome. Apropos of 2 cases over 3 generations].

Poissonnier M, Andrieu J, Gardon JD, Saint-Martin JL, Gruyer P, Martignon C. Poissonnier M, et al. J Genet Hum. 1983 Dec;31(4):255-78. J Genet Hum. 1983. PMID: 6663287 French.

6

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

Rahmani Z, Blouin JL, Creau-Goldberg N, Watkins PC, Mattei JF, Poissonnier M, Prieur M, Chettouh Z, Nicole A, Aurias A, et al. Rahmani Z, et al. Among authors: poissonnier m. Proc Natl Acad Sci U S A. 1989 Aug;86(15):5958-62. doi: 10.1073/pnas.86.15.5958. Proc Natl Acad Sci U S A. 1989. PMID: 2527368 Free PMC article.

7

Down syndrome critical region around D21S55 on proximal 21q22.3.

Rahmani Z, Blouin JL, Créau-Goldberg N, Watkins PC, Mattei JF, Poissonnier M, Prieur M, Chettouh Z, Nicole A, Aurias A, et al. Rahmani Z, et al. Among authors: poissonnier m. Am J Med Genet Suppl. 1990;7:98-103. doi: 10.1002/ajmg.1320370720. Am J Med Genet Suppl. 1990. PMID: 2149984

8

[True hermaphroditism in a child with a chimeric XX/XY chromosome, a double erythrocyte population and an unusual Lewis (a+ b+) phenotype].

Poissonnier M, Janvier D, Cabrol S, Reviron M, Noël L, Reviron J. Poissonnier M, et al. J Genet Hum. 1987 May;35(2-3):119-29. J Genet Hum. 1987. PMID: 3612092 French.

9

Acute lymphoblastic leukemia with trisomy 21 constitutional mosaicism.

Léonard C, Avalos MR, Miélot F, Poissonnier M, Dommergues JP, Lejeune J, Tchernia G. Léonard C, et al. Among authors: poissonnier m. Cancer Genet Cytogenet. 1993 Mar;66(1):70-2. doi: 10.1016/0165-4608(93)90151-b. Cancer Genet Cytogenet. 1993. PMID: 8467478

10

[Partial trisomy 21 (21q21 - 21q22.2)].

Poissonnier M, Saint-Paul B, Dutrillaux B, Chassaigne M, Gruyer P, de Blignières-Strouk G. Poissonnier M, et al. Ann Genet. 1976 Mar;19(1):69-73. Ann Genet. 1976. PMID: 132130 French.

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