122 related articles for article (PubMed ID: 6114032)
21. [Aniridia and deletion of chromosome 11 (loss of the band p13)--apropos of a case].
Raspiller A; Gilgenkrantz S; Pernot C; Lardenet F
Bull Soc Ophtalmol Fr; 1982; 82(8-9):1155-7. PubMed ID: 7165953
[No Abstract] [Full Text] [Related]
22. Ambiguous genitalia, gonadoblastoma, aniridia and mental retardation with deletion of chromosome 11.
Martinez-Mora J; Audi L; Toran N; Isnard R; Castellvi A; Perez Iribarne M; Egozcue J
J Urol; 1989 Nov; 142(5):1298-300. PubMed ID: 2810512
[TBL] [Abstract][Full Text] [Related]
23. Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome.
Reardon W; Gibbons RJ; Winter RM; Baraitser M
Am J Med Genet; 1995 Jan; 55(3):285-7. PubMed ID: 7726224
[TBL] [Abstract][Full Text] [Related]
24. Male pseudohermaphroditism, partial androgen receptors defect, 11p13 deletion: indication of gene localization.
Malpuech G; Sultan C; Bertheas MF; Loire C; Renaud H; Francannet C; Vanlieferinghen P
Am J Med Genet; 1986 Aug; 24(4):679-84. PubMed ID: 3017106
[TBL] [Abstract][Full Text] [Related]
25. Catalase levels in patients with aniridia and/or Wilms' tumor: utility and limitations.
Ferrell RE; Riccardi VM
Cytogenet Cell Genet; 1981; 31(2):120-3. PubMed ID: 6273073
[TBL] [Abstract][Full Text] [Related]
26. Clinical features of monosomy 10qter.
Zatterale A; Pagano L; Fioretti G; Caniglia M; Festa B; Renda S; Rinaldi MM; Ventruto V
Ann Genet; 1983; 26(2):106-8. PubMed ID: 6604483
[TBL] [Abstract][Full Text] [Related]
27. Aniridia caused by a heritable chromosome 11 deletion.
Hittner HM; Riccardi VM; Francke U
Ophthalmology; 1979 Jun; 86(6):1173-83. PubMed ID: 230439
[TBL] [Abstract][Full Text] [Related]
28. Aniridia and interstitial deletion of the short arm of chromosome 11.
Warburg M; Mikkelsen M; Andersen SR; Geertinger P; Larsen HW; Vestermark S; Parving A
Metab Pediatr Ophthalmol; 1980; 4(2):97-102. PubMed ID: 7442353
[No Abstract] [Full Text] [Related]
29. [A case of male pseudohermaphroditism with structural abnormalities of Y chromosome (ring Y)].
Watanabe H; Hachisuka Y; Watase H; Fushimi N; Ohtaguro K
Hinyokika Kiyo; 1988 Aug; 34(8):1469-74. PubMed ID: 3057830
[TBL] [Abstract][Full Text] [Related]
30. 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
Genes Chromosomes Cancer; 1993 May; 7(1):57-62. PubMed ID: 7688557
[TBL] [Abstract][Full Text] [Related]
31. [Bilateral nephroblastoma with aniridia].
Weyl M; Brichon P; Leturgeon MC; Alison M
Arch Fr Pediatr; 1986 Feb; 43(2):119-21. PubMed ID: 3013116
[TBL] [Abstract][Full Text] [Related]
32. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
[TBL] [Abstract][Full Text] [Related]
33. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).
Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F
Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646
[TBL] [Abstract][Full Text] [Related]
34. [WAGR syndrome: a case report].
Moreno García M; Sánchez del Pozo J; Fernández Martínez FJ; Moreno-Izquierdo A; Barreiro Miranda E
An Esp Pediatr; 1998 Oct; 49(4):381-7. PubMed ID: 9859552
[TBL] [Abstract][Full Text] [Related]
35. A patient with dup(10p)del(8q) and Pendred syndrome.
van Wouwe JP; Wijnands MC; Mourad-Baars PE; Geraedts JP; Beverstock GC; van de Kamp JJ
Am J Med Genet; 1986 Jun; 24(2):211-7. PubMed ID: 3717206
[TBL] [Abstract][Full Text] [Related]
36. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
Steinbach P; Wolf M; Schmidt H
Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
[TBL] [Abstract][Full Text] [Related]
37. 18q- and 18q+ mosaicism in a mentally retarded boy.
Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
[TBL] [Abstract][Full Text] [Related]
38. Interstitial del(13q) associated with blindness and mental retardation.
Juberg RC; Mowrey PN
Am J Med Genet; 1984 Mar; 17(3):609-13. PubMed ID: 6711612
[TBL] [Abstract][Full Text] [Related]
39. Familial deletion.
Smith A; Murray R; Den Dulk G
Ann Genet; 1983; 26(2):91-3. PubMed ID: 6604492
[TBL] [Abstract][Full Text] [Related]
40. Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)].
Moore JW; Hyman S; Antonarakis SE; Mules EH; Thomas GH
Hum Genet; 1986 Apr; 72(4):297-302. PubMed ID: 3754537
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
