Henry I - Search Results

1

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: henry i. Hum Genet. 1994 Jul;94(1):88-90. doi: 10.1007/BF02272849. Hum Genet. 1994. PMID: 8034301

2

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. Hum Genet. 1989 Feb;81(3):273-7. doi: 10.1007/BF00279003. Hum Genet. 1989. PMID: 2921038

3

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. Cytogenet Cell Genet. 1989;50(2-3):155-7. doi: 10.1159/000132748. Cytogenet Cell Genet. 1989. PMID: 2550179

4

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. 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.

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: henry i. Hum Genet. 1989 May;82(2):171-8. doi: 10.1007/BF00284053. Hum Genet. 1989. PMID: 2722195

6

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. Among authors: henry i. Hum Genet. 1987 Nov;77(3):283-5. doi: 10.1007/BF00284487. Hum Genet. 1987. PMID: 2824335

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. Genes Chromosomes Cancer. 1993 May;7(1):57-62. doi: 10.1002/gcc.2870070110. Genes Chromosomes Cancer. 1993. PMID: 7688557 Free article.

8

Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event.

Henry I, Puech A, Riesewijk A, Ahnine L, Mannens M, Beldjord C, Bitoun P, Tournade MF, Landrieu P, Junien C. Henry I, et al. Eur J Hum Genet. 1993;1(1):19-29. doi: 10.1159/000472384. Eur J Hum Genet. 1993. PMID: 8069648

9

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.

Jeanpierre C, Denamur E, Henry I, Cabanis MO, Luce S, Cécille A, Elion J, Peuchmaur M, Loirat C, Niaudet P, Gubler MC, Junien C. Jeanpierre C, et al. Among authors: henry i. Am J Hum Genet. 1998 Apr;62(4):824-33. doi: 10.1086/301806. Am J Hum Genet. 1998. PMID: 9529364 Free PMC article.

10

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

Moutou C, Junien C, Henry I, Bonaïti-Pellié C. Moutou C, et al. Among authors: henry i. J Med Genet. 1992 Apr;29(4):217-20. doi: 10.1136/jmg.29.4.217. J Med Genet. 1992. PMID: 1583638 Free PMC article.

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