162 related articles for article (PubMed ID: 2921037)
1. Incontinentia pigmenti and X-autosome translocations. Non-isotopic in situ hybridization with an X-centromere-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in one of five published cases.
Crolla JA; Gilgenkrantz S; de Grouchy J; Kajii T; Bobrow M
Hum Genet; 1989 Feb; 81(3):269-72. PubMed ID: 2921037
[TBL] [Abstract][Full Text] [Related]
2. Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation.
Cannizzaro LA; Hecht F
Clin Genet; 1987 Jul; 32(1):66-9. PubMed ID: 3621656
[TBL] [Abstract][Full Text] [Related]
3. The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localization.
Harris A; Lankester S; Haan E; Beres J; Hulten M; Szollar J; Souttier L; Bobrow M
Clin Genet; 1988 Jul; 34(1):1-6. PubMed ID: 2900707
[TBL] [Abstract][Full Text] [Related]
4. Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations.
Sefiani A; Heuertz S; Turleau C; Thibaud D; de Grouchy J; Hors-Cayla MC
Ann Genet; 1989; 32(3):149-51. PubMed ID: 2817774
[TBL] [Abstract][Full Text] [Related]
5. Two cases of X/autosome translocation in females with incontinentia pigmenti.
Hodgson SV; Neville B; Jones RW; Fear C; Bobrow M
Hum Genet; 1985; 71(3):231-4. PubMed ID: 4065895
[TBL] [Abstract][Full Text] [Related]
6. Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): implications for the regional assignment of the IP locus to Xp11?
Gilgenkrantz S; Tridon P; Pinel-Briquel N; Beurey J; Weber M
Ann Genet; 1985; 28(2):90-2. PubMed ID: 3876069
[TBL] [Abstract][Full Text] [Related]
7. Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints.
Gorski JL; Burright EN; Harnden CE; Stein CK; Glover TW; Reyner EL
Am J Hum Genet; 1991 Jan; 48(1):53-64. PubMed ID: 1985463
[TBL] [Abstract][Full Text] [Related]
8. A somatic cell hybrid panel to facilitate identification of DNA sequences in the vicinity of the incontinentia pigmenti locus (IP1).
Gorski JL; Stein CK; Glover TW
Cytogenet Cell Genet; 1989; 52(1-2):90-2. PubMed ID: 2558857
[TBL] [Abstract][Full Text] [Related]
9. Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.
Sefiani A; Sinnett D; Abel L; Szpiro-Tapia S; Heuertz S; Craig I; Fraser N; Kruse TA; Frydman M; Peter MO
Hum Genet; 1988 Nov; 80(3):282-6. PubMed ID: 3192215
[TBL] [Abstract][Full Text] [Related]
10. Incontinentia pigmenti (type 1) and X;5 translocation.
Bitoun P; Philippe C; Cherif M; Mulcahy MT; Gilgenkrantz S
Ann Genet; 1992; 35(1):51-4. PubMed ID: 1610121
[TBL] [Abstract][Full Text] [Related]
11. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
Gorski JL; Bialecki MD; McDonald MT; Massa HF; Trask BJ; Burright EN
Genomics; 1996 Jul; 35(2):338-45. PubMed ID: 8661147
[TBL] [Abstract][Full Text] [Related]
12. Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11.
Koiffmann CP; de Souza DH; Diament A; Ventura HB; Alves RS; Kihara S; Wajntal A
Am J Med Genet; 1993 Jun; 46(5):529-33. PubMed ID: 8322815
[TBL] [Abstract][Full Text] [Related]
13. Incontinentia pigmenti in a boy with Klinefelter's syndrome.
Ormerod AD; White MI; McKay E; Johnston AW
J Med Genet; 1987 Jul; 24(7):439-41. PubMed ID: 3612722
[TBL] [Abstract][Full Text] [Related]
14. Recent progress in the genetics of incontinentia pigmenti (Bloch-Sulzberger syndrome).
Shastry BS
J Hum Genet; 2000; 45(6):323-6. PubMed ID: 11185738
[TBL] [Abstract][Full Text] [Related]
15. Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric region.
de Grouchy J; Turleau C; Doussau de Bazignan M; Maroteaux P; Thibaud D
Ann Genet; 1985; 28(2):86-9. PubMed ID: 3876068
[TBL] [Abstract][Full Text] [Related]
16. The gene for incontinentia pigmenti is assigned to Xq28.
Sefiani A; Abel L; Heuertz S; Sinnett D; Lavergne L; Labuda D; Hors-Cayla MC
Genomics; 1989 Apr; 4(3):427-9. PubMed ID: 2714798
[TBL] [Abstract][Full Text] [Related]
17. Incontinentia pigmenti in a male infant with Klinefelter syndrome.
Prendiville JS; Gorski JL; Stein CK; Esterly NB
J Am Acad Dermatol; 1989 May; 20(5 Pt 2):937-40. PubMed ID: 2715449
[TBL] [Abstract][Full Text] [Related]
18. Clinical features and computer-aided analysis of chromosome aberration in a case with incontinentia pigmenti.
Parcheta B; Skawinski W; Wisniewski L; Piontek E; Ryzko J
Klin Padiatr; 1987; 199(1):32-6. PubMed ID: 3550261
[TBL] [Abstract][Full Text] [Related]
19. Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.
Hydén-Granskog C; Salonen R; von Koskull H
Hum Genet; 1993 Mar; 91(2):185-9. PubMed ID: 8096494
[TBL] [Abstract][Full Text] [Related]
20. Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma.
Kajii T; Tsukahara M; Fukushima Y; Hata A; Matsuo K; Kuroki Y
Ann Genet; 1985; 28(4):219-23. PubMed ID: 3879432
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
