Babin P - Search Results

1

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: babin p. Hum Genet. 1991 Jul;87(3):317-9. doi: 10.1007/BF00200911. Hum Genet. 1991. PMID: 1864606

2

Translocation (8;9)(q12;p21). A new non-random rearrangement in lymphoid malignancies.

Huret JL, Brizard A, Babin P, Schoënwald M, Briault S, Guilhot F, Tanzer J. Huret JL, et al. Among authors: babin p. Cancer Genet Cytogenet. 1990 Mar;45(1):125-9. doi: 10.1016/0165-4608(90)90075-l. Cancer Genet Cytogenet. 1990. PMID: 2302679

3

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: babin p. Blood. 1988 Sep;72(3):1045-7. Blood. 1988. PMID: 3416066 Free article.

4

The naevoid basal-cell carcinoma syndrome (Gorlin syndrome) is a chromosomal instability syndrome.

Shafei-Benaissa E, Savage JR, Babin P, Larrègue M, Papworth D, Tanzer J, Bonnetblanc JM, Huret JL. Shafei-Benaissa E, et al. Among authors: babin p. Mutat Res. 1998 Feb 2;397(2):287-92. doi: 10.1016/s0027-5107(97)00228-5. Mutat Res. 1998. PMID: 9541654

5

Evidence of chromosomal instability in the lymphocytes of Gorlin basal-cell carcinoma patients.

Shafei-Benaissa E, Savage JR, Papworth D, Babin P, Larrègue M, Tanzer J, Bonnetblanc JM, Vaillant L, Huret JL. Shafei-Benaissa E, et al. Among authors: babin p. Mutat Res. 1995 Nov;332(1-2):27-32. doi: 10.1016/0027-5107(95)00082-0. Mutat Res. 1995. PMID: 7500988

6

Checks for chromosomal instability in Gorlin and non-Gorlin basal-cell carcinoma patients.

Shafei-Benaissa E, Huret JL, Larrègue M, Babin P, Tanzer J, Decrozailles JM, Savage JR. Shafei-Benaissa E, et al. Among authors: babin p. Mutat Res. 1994 Jul 1;308(1):1-9. doi: 10.1016/0027-5107(94)90193-7. Mutat Res. 1994. PMID: 7516477

7

Four additional cases of trisomy 14 as the sole anomaly in various haematological malignancies.

Brizard A, Guilhot F, Babin P, Burucoa C, Tanzer J, Huret JL. Brizard A, et al. Among authors: babin p. Leuk Res. 1992;16(5):537-40. doi: 10.1016/0145-2126(92)90181-6. Leuk Res. 1992. PMID: 1625480 Review.

8

Karyotypes of 33 patients with clonal aberrations in chronic lymphocytic leukaemia. Review of 216 abnormal karyotypes in chronic lymphocytic leukaemia.

Huret JL, Mossafa H, Brizard A, Dreyfus B, Guilhot F, Xue XQ, Babin P, Tanzer J. Huret JL, et al. Among authors: babin p. Ann Genet. 1989;32(3):155-9. Ann Genet. 1989. PMID: 2817776

9

A case of inv(5) in non-Hodgkin's lymphoma.

Huret JL, Guilhot F, Brizard A, Briault S, Babin P, Tanzer J. Huret JL, et al. Among authors: babin p. Cancer Genet Cytogenet. 1989 Feb;37(2):279-80. doi: 10.1016/0165-4608(89)90060-5. Cancer Genet Cytogenet. 1989. PMID: 2702628 No abstract available.

10

Translocation t(12;13)(p13.3;q12.2) is Not Restricted to Lymphoid Malignancies; Report of a Further Case with Hypereosinophilia.

Huret JL, Brizard A, Benz-Lemoine E, Babin P, Desmarest MC, Demeure L, Tanzer J. Huret JL, et al. Among authors: babin p. Leuk Lymphoma. 1991;4(3):211-3. doi: 10.3109/10428199109068067. Leuk Lymphoma. 1991. PMID: 27458675

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