Detalhe da pesquisa
1.
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants.
J Genet Couns
; 2023 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37282361
2.
Birt-Hogg-Dubé syndrome: clinical and genetic studies of 10 French families.
Br J Dermatol
; 162(3): 527-37, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19785621
3.
The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Br J Cancer
; 101(8): 1456-60, 2009 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-19707196
4.
[Hereditary predispositions to gynaecological cancers]. / Prédispositions héréditaires aux cancers gynécologiques.
Gynecol Obstet Fertil
; 33(11): 851-6, 2005 Nov.
Artigo
em Francês
| MEDLINE | ID: mdl-16256400
5.
Structural and numerical aberrations of chromosome 22 in a case of follicular variant of papillary thyroid carcinoma revealed by conventional and molecular cytogenetics.
Cancer Genet Cytogenet
; 121(1): 33-7, 2000 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10958938
6.
[Infant rhabdoid tumors: a diagnostic emergency]. / Tumeurs rhabdoïdes du nourrisson : une urgence diagnostique.
Arch Pediatr
; 21(11): 1246-9, 2014 Nov.
Artigo
em Francês
| MEDLINE | ID: mdl-25267195
7.
[Genetic predisposition to childhood cancer]. / Oncogénétique en oncopédiatrie.
Arch Pediatr
; 19(8): 863-75, 2012 Aug.
Artigo
em Francês
| MEDLINE | ID: mdl-22796286
8.
Bar code screening on combed DNA for large rearrangements of the BRCA1 and BRCA2 genes in French breast cancer families.
J Med Genet
; 39(11): 817-21, 2002 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12414821
9.
[Cowden syndrome, or multiple hamartomatous tumor syndrome, in clinical endocrinology]. / Le syndrome de Cowden ou syndrome des hamartomes multiples en endocrinologie clinique.
Ann Endocrinol (Paris)
; 71(4): 264-73, 2010 Sep.
Artigo
em Francês
| MEDLINE | ID: mdl-20627233
10.
Acute lymphocytic leukaemia in a child with Beckwith-Wiedemann syndrome harbouring a CDKN1C mutation.
Eur J Med Genet
; 53(6): 400-3, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20826236
11.
An unusual succinate dehydrogenase gene mutation C in a case of laryngeal paraganglioma.
J Laryngol Otol
; 123(1): 141-4, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18267044