Barichard F - Search Results

1

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

Henry I, Grandjouan S, Couillin P, Barichard F, Huerre-Jeanpierre C, Glaser T, Philip T, Lenoir G, Chaussain JL, Junien C. Henry I, et al. Among authors: barichard f. Proc Natl Acad Sci U S A. 1989 May;86(9):3247-51. doi: 10.1073/pnas.86.9.3247. Proc Natl Acad Sci U S A. 1989. PMID: 2566168 Free PMC article.

2

Mitotic deletions of 11p15.5 in two different tumors indicate that the CALCA locus is distal to the PTH locus.

Henry I, Grandjouan S, Barichard F, Huerre-Jeanpierre C, Junien C. Henry I, et al. Among authors: barichard f. Cytogenet Cell Genet. 1989;50(2-3):155-7. doi: 10.1159/000132748. Cytogenet Cell Genet. 1989. PMID: 2550179

3

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma.

Henry I, Jeanpierre M, Couillin P, Barichard F, Serre JL, Journel H, Lamouroux A, Turleau C, de Grouchy J, Junien C. Henry I, et al. Among authors: barichard f. Hum Genet. 1989 Feb;81(3):273-7. doi: 10.1007/BF00279003. Hum Genet. 1989. PMID: 2921038

4

Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.

Lavedan C, Barichard F, Azoulay M, Couillin P, Molina Gomez D, Nicolas H, Quack B, Rethoré MO, Noel B, Junien C. Lavedan C, et al. Among authors: barichard f. Cytogenet Cell Genet. 1989;50(2-3):70-4. doi: 10.1159/000132726. Cytogenet Cell Genet. 1989. PMID: 2570677

5

Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex region.

Couillin P, Azoulay M, Henry I, Ravisé N, Grisard MC, Jeanpierre C, Barichard F, Metezeau P, Candelier JJ, Lewis W, et al. Couillin P, et al. Among authors: barichard f. Hum Genet. 1989 May;82(2):171-8. doi: 10.1007/BF00284053. Hum Genet. 1989. PMID: 2722195

6

Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome.

Henry I, Jeanpierre M, Barichard F, Serre JL, Mallet J, Turleau C, de Grouchy J, Junien C. Henry I, et al. Among authors: barichard f. Ann Genet. 1988;31(4):216-20. Ann Genet. 1988. PMID: 2905880

7

Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family.

Henry I, Hoovers J, Barichard F, Berthéas MF, Puech A, Prieur F, Gessler M, Bruns G, Mannens M, Junien C. Henry I, et al. Among authors: barichard f. Genes Chromosomes Cancer. 1993 May;7(1):57-62. doi: 10.1002/gcc.2870070110. Genes Chromosomes Cancer. 1993. PMID: 7688557 Free article.

8

Single base pair germ-line deletion in the p53 gene in a cancer predisposed family.

Hamelin R, Barichard F, Henry I, Junien C, Thomas G. Hamelin R, et al. Among authors: barichard f. Hum Genet. 1994 Jul;94(1):88-90. doi: 10.1007/BF02272849. Hum Genet. 1994. PMID: 8034301

9

Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34----7q22.

Barichard F, Joulin V, Henry I, Garel MC, Valentin C, Rosa R, Cohen-Solal M, Junien C. Barichard F, et al. Hum Genet. 1987 Nov;77(3):283-5. doi: 10.1007/BF00284487. Hum Genet. 1987. PMID: 2824335

10

Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1.

Henry I, Bernheim A, Bernard M, van der Rest M, Kimura T, Jeanpierre C, Barichard F, Berger R, Olsen BR, Ramirez F, et al. Henry I, et al. Among authors: barichard f. Genomics. 1988 Jul;3(1):87-90. doi: 10.1016/0888-7543(88)90165-6. Genomics. 1988. PMID: 3220479

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