122 related articles for article (PubMed ID: 6114032)
1. Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.
Turleau C; de Grouchy J; Dufier JL; Phuc LH; Schmelck PH; Rappaport R; Nihoul-Fékété C; Diebold N
Hum Genet; 1981; 57(3):300-6. PubMed ID: 6114032
[TBL] [Abstract][Full Text] [Related]
2. Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.
Turleau C; de Grouchy J; Dufier JL; Lè Hoang P; Schmelck PH; Rappaport R; Nihoul-Fékété C; Diebold N
Hum Genet; 1981 May; 57(3):300-306. PubMed ID: 28035502
[TBL] [Abstract][Full Text] [Related]
3. Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.
Junien C; Turleau C; de Grouchy J; Saïd R; Rethoré MO L; Tenconi R; Dufier JL
Ann Genet; 1980; 23(3):165-8. PubMed ID: 6252821
[TBL] [Abstract][Full Text] [Related]
4. [Intercalary deletion of the short arm of chromosome 11: aniridia, glaucoma, staturoponderal and mental retardation, sexual ambiguity, gonadoblastoma and catalase deficiency].
Dufier JL; Phug LH; Schmelck P; Fekete C; de Grouchy J; Turleau C; Haye C
Bull Soc Ophtalmol Fr; 1981 Oct; 81(10):747-9. PubMed ID: 7332973
[No Abstract] [Full Text] [Related]
5. [WAGR syndrome, Wilms' tumor, aniridia, gonadoblastoma, mental retardation: a review apropos of 2 cases].
Mochon MC; Blanc JF; Plauchu H; Philip T
Pediatrie; 1987; 42(4):249-52. PubMed ID: 2823214
[TBL] [Abstract][Full Text] [Related]
6. [P 11 deletion syndrome. Aniridia, urogenital malformation and mental retardation].
Andersen SR; Geertinger P; Larsen HW; Mikkelsen M; Vestermark S; Warburg M
Ugeskr Laeger; 1978 Aug; 140(35):2112. PubMed ID: 211686
[No Abstract] [Full Text] [Related]
7. Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathy.
Gilgenkrantz S; Vigneron C; Gregoire MJ; Pernot C; Raspiller A
Am J Med Genet; 1982 Sep; 13(1):39-49. PubMed ID: 6127950
[TBL] [Abstract][Full Text] [Related]
8. Complete and partial XY sex reversal associated with terminal deletion of 10q: report of 2 cases and literature review.
Wilkie AO; Campbell FM; Daubeney P; Grant DB; Daniels RJ; Mullarkey M; Affara NA; Fitchett M; Huson SM
Am J Med Genet; 1993 Jun; 46(5):597-600. PubMed ID: 8322827
[TBL] [Abstract][Full Text] [Related]
9. Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.
Narahara K; Kikkawa K; Kimira S; Kimoto H; Ogata M; Kasai R; Hamawaki M; Matsuoka K
Hum Genet; 1984; 66(2-3):181-5. PubMed ID: 6325323
[TBL] [Abstract][Full Text] [Related]
10. Chromosome abnormalities involving 11p13 and low erythrocyte catalase activity.
Niikawa N; Fukushima Y; Taniguchi N; Iizuka S; Kajii T
Hum Genet; 1982; 60(4):373-5. PubMed ID: 7106775
[TBL] [Abstract][Full Text] [Related]
11. Aniridia, cataract and gonadoblastoma in a mentally retarded girl with deletion of chromosome II. A clinicopathological case report.
Andersen SR; Geertinger P; Larsen HW; Mikkelsen M; Parving A; Vestermark S; Warburg M
Ophthalmologica; 1977; 176(3):171-7. PubMed ID: 613291
[TBL] [Abstract][Full Text] [Related]
12. Aniridia and mental retardation with deletion of the short arm of chromosome 11.
Kaiser-Kupfer MI; White BJ; Papadopoulos N
Trans Am Ophthalmol Soc; 1981; 79():276-93. PubMed ID: 7342404
[No Abstract] [Full Text] [Related]
13. 11p13 deletion and reduced RBC catalase in a patient with aniridia, glaucoma and bilateral Wilms' tumor.
Barletta C; Castello MA; Ferrante E; Mavelli I; Clerico A; Ciriolo MR; Vignetti P
Tumori; 1985 Apr; 71(2):119-21. PubMed ID: 2988163
[TBL] [Abstract][Full Text] [Related]
14. [Chromosome 11 and cancer].
Gregoire MJ; Pernot C; Himont F; Pierson M; Gilgenkrantz S
J Genet Hum; 1983 Mar; 31(1):31-6. PubMed ID: 6311963
[TBL] [Abstract][Full Text] [Related]
15. Abnormalities of human autosomes. I. Ambigous genitalia associated with a translocation 46,XY, t(Cq+;Cq-).
German J; Simpson JL
Birth Defects Orig Artic Ser; 1971 May; 7(6):145-9. PubMed ID: 5173157
[TBL] [Abstract][Full Text] [Related]
16. Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature.
Turleau C; de Grouchy J; Tournade MF; Gagnadoux MF; Junien C
Clin Genet; 1984 Oct; 26(4):356-62. PubMed ID: 6094051
[TBL] [Abstract][Full Text] [Related]
17. Del11p13/nephroblastoma without aniridia.
Turleau C; de Grouchy J; Nihoul-Fékété C; Dufier JL; Chavin-Colin F; Junien C
Hum Genet; 1984; 67(4):455-6. PubMed ID: 6092262
[TBL] [Abstract][Full Text] [Related]
18. Aniridia: enzyme studies in an 11p--chromosomal deletion.
Bateman JB; Sparkes MC; Sparkes RS
Invest Ophthalmol Vis Sci; 1984 May; 25(5):612-6. PubMed ID: 6325367
[TBL] [Abstract][Full Text] [Related]
19. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
[TBL] [Abstract][Full Text] [Related]
20. A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features.
Hoffer MJ; Hilhorst-Hofstee Y; Knijnenburg J; Hansson KB; Engelberts AC; Laan LA; Bakker E; Rosenberg C
Eur J Med Genet; 2007; 50(2):149-54. PubMed ID: 17223398
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
