Couet D - Search Results

1

INV(12) (p13q11) and dicentric chromosomes in a secondary leukaemia with basophilia.

Huret JL, Brizard A, Guilhot F, Couet D, Schoenwald M, Savage JR, Tanzer J. Huret JL, et al. Among authors: couet d. Haematologica. 1990 Sep-Oct;75(5):473-6. Haematologica. 1990. PMID: 2129034

2

Malignant histiocytosis: a specific t(2;5)(p23;q35) translocation? Review of the literature.

Benz-Lemoine E, Brizard A, Huret JL, Babin P, Guilhot F, Couet D, Tanzer J. Benz-Lemoine E, et al. Among authors: couet d. Blood. 1988 Sep;72(3):1045-7. Blood. 1988. PMID: 3416066 Free article.

3

Aberrant translocations in chronic myelogenous leukaemia with hidden chromosome 9 or 22 involvement.

Huret JL, Bresson JL, Couet D, Tanzer J. Huret JL, et al. Among authors: couet d. Ann Genet. 1987;30(3):175-7. Ann Genet. 1987. PMID: 3499856

4

Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotype.

Bonneau D, Huret JL, Godeau G, Couet D, Putterman M, Tanzer J, Babin P, Larrègue M. Bonneau D, et al. Among authors: couet d. Hum Genet. 1991 Jul;87(3):317-9. doi: 10.1007/BF00200911. Hum Genet. 1991. PMID: 1864606

5

A two-step t(4;der(15)) t(15;17) complex translocation in an acute promyelocytic leukaemia and review of the literature.

Huret JL, Couet D, Guilhot F, Brizard A, Tanzer J. Huret JL, et al. Among authors: couet d. Leuk Res. 1987;11(8):761-5. doi: 10.1016/0145-2126(87)90014-2. Leuk Res. 1987. PMID: 3306169 Review. No abstract available.

6

Aplasia cutis congenita of the scalp in an infant exposed to valproic acid in utero.

Hubert A, Bonneau D, Couet D, Berthier M, Oriot D, Larrègue M. Hubert A, et al. Among authors: couet d. Acta Paediatr. 1994 Jul;83(7):789-90. doi: 10.1111/j.1651-2227.1994.tb13143.x. Acta Paediatr. 1994. PMID: 7949818

7

Obesity: a new feature of WAGR (del 11p) syndrome.

Marlin S, Couet D, Lacombe D, Cessans C, Bonneau D. Marlin S, et al. Among authors: couet d. Clin Dysmorphol. 1994 Jul;3(3):255-7. Clin Dysmorphol. 1994. PMID: 7526938

8

Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.

Lacombe D, Bonneau D, Verloes A, Couet D, Koulischer L, Battin J. Lacombe D, et al. Among authors: couet d. Genet Couns. 1993;4(3):193-8. Genet Couns. 1993. PMID: 8267926

9

Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.

Naoufal R, Legendre M, Couet D, Gilbert-Dussardier B, Kitzis A, Bilan F, Harbuz R. Naoufal R, et al. Among authors: couet d. Eur J Med Genet. 2016 Sep;59(9):483-7. doi: 10.1016/j.ejmg.2016.07.001. Epub 2016 Jul 21. Eur J Med Genet. 2016. PMID: 27452446

10

Osteogenesis imperfecta, tricho-dento-osseous syndrome and intellectual disability: a familial case with 17q21.33-q22 (COL1A1 and DLX3) deletion and 7q32.3-q33 duplication resulting from a reciprocal interchromosomal insertion.

Harbuz R, Bilan F, Couet D, Charraud V, Kitzis A, Gilbert-Dussardier B. Harbuz R, et al. Among authors: couet d. Am J Med Genet A. 2013 Oct;161A(10):2504-11. doi: 10.1002/ajmg.a.36122. Epub 2013 Aug 15. Am J Med Genet A. 2013. PMID: 23949819

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