120 related articles for article (PubMed ID: 1754556)
1. Prenatal diagnosis of PIBIDS.
Savary JB; Vasseur F; Vinatier D; Manouvrier S; Thomas P; Deminatti MM
Prenat Diagn; 1991 Nov; 11(11):859-66. PubMed ID: 1754556
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair.
Sarasin A; Blanchet-Bardon C; Renault G; Lehmann A; Arlett C; Dumez Y
Br J Dermatol; 1992 Nov; 127(5):485-91. PubMed ID: 1281671
[TBL] [Abstract][Full Text] [Related]
3. First-trimester prenatal exclusion of PIBIDS syndrome with normal DNA excision repair on chorionic villus cells.
Savary JB; Vasseur F; Vinatier D; Manouvrier S; Deminatti MM
Prenat Diagn; 1992 Nov; 12(11):969-71. PubMed ID: 1494551
[No Abstract] [Full Text] [Related]
4. The comet assay as a repair test for prenatal diagnosis of Xeroderma pigmentosum and trichothiodystrophy.
Alapetite C; Benoit A; Moustacchi E; Sarasin A
J Invest Dermatol; 1997 Feb; 108(2):154-9. PubMed ID: 9008227
[TBL] [Abstract][Full Text] [Related]
5. Routine autoradiographic analysis of DNA excision-repair. Report of prenatal and postnatal diagnosis in eleven families.
Savary JB; Vasseur F; Deminatti MM
Ann Genet; 1991; 34(2):76-81. PubMed ID: 1746887
[TBL] [Abstract][Full Text] [Related]
6. [Trichothiodystrophy: PIBIDS syndrome].
Jiménez-Puya R; Moreno-Giménez JC; Camacho-Martínez F; Ferrando-Barbera J; Grimalt R
Actas Dermosifiliogr; 2007 Apr; 98(3):183-7. PubMed ID: 17504703
[TBL] [Abstract][Full Text] [Related]
7. Short stature with congenital ichthyosis.
Lakhani SJ; Lakhani OJ
BMJ Case Rep; 2015 Dec; 2015():. PubMed ID: 26661284
[TBL] [Abstract][Full Text] [Related]
8. Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity.
Stefanini M; Lagomarsini P; Giorgi R; Nuzzo F
Mutat Res; 1987 Jun; 191(2):117-9. PubMed ID: 3600693
[TBL] [Abstract][Full Text] [Related]
9. Prenatal exclusion of harlequin ichthyosis; potential pitfalls in the timing of the fetal skin biopsy.
Shimizu A; Akiyama M; Ishiko A; Yoshiike T; Suzumori K; Shimizu H
Br J Dermatol; 2005 Oct; 153(4):811-4. PubMed ID: 16181466
[TBL] [Abstract][Full Text] [Related]
10. Characteristic morphologic abnormality of harlequin ichthyosis detected in amniotic fluid cells.
Akiyama M; Kim DK; Main DM; Otto CE; Holbrook KA
J Invest Dermatol; 1994 Feb; 102(2):210-3. PubMed ID: 8106750
[TBL] [Abstract][Full Text] [Related]
11. Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.
de Boer J; van Steeg H; Berg RJ; Garssen J; de Wit J; van Oostrum CT; Beems RB; van der Horst GT; van Kreijl CF; de Gruijl FR; Bootsma D; Hoeijmakers JH; Weeda G
Cancer Res; 1999 Jul; 59(14):3489-94. PubMed ID: 10416615
[TBL] [Abstract][Full Text] [Related]
12. [Trichothiodystrophy: progresssive manifestations].
Foulc P; Jumbou O; David A; Sarasin A; Stalder JF
Ann Dermatol Venereol; 1999 Oct; 126(10):703-7. PubMed ID: 10604009
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of vitamin D-dependent rickets, type II: response to 1,25-dihydroxyvitamin D in amniotic fluid cells and fetal tissues.
Weisman Y; Jaccard N; Legum C; Spirer Z; Yedwab G; Even L; Edelstein S; Kaye AM; Hochberg Z
J Clin Endocrinol Metab; 1990 Oct; 71(4):937-43. PubMed ID: 2169482
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of harlequin ichthyosis by the examination of keratinized hair canals and amniotic fluid cells at 19 weeks' estimated gestational age.
Akiyama M; Suzumori K; Shimizu H
Prenat Diagn; 1999 Feb; 19(2):167-71. PubMed ID: 10215076
[TBL] [Abstract][Full Text] [Related]
15. Trichothiodystrophy: Photosensitive, TTD-P, TTD, Tay syndrome.
Lambert WC; Gagna CE; Lambert MW
Adv Exp Med Biol; 2010; 685():106-10. PubMed ID: 20687499
[TBL] [Abstract][Full Text] [Related]
16. Trichothiodystrophy: report of a new case with severe nervous system impairment.
Rizzo R; Pavone L; Micali G; Calvieri S; Di Gregorio L
J Child Neurol; 1992 Jul; 7(3):300-3. PubMed ID: 1634754
[No Abstract] [Full Text] [Related]
17. Prenatal diagnosis of Cockayne syndrome using assay of colony-forming ability in ultraviolet light irradiated cells.
Sugita T; Ikenaga M; Suehara N; Kozuka T; Furuyama J; Yabuuchi H
Clin Genet; 1982 Sep; 22(3):137-42. PubMed ID: 7151298
[No Abstract] [Full Text] [Related]
18. Prenatal diagnosis of del(11)(p13p15).
Stern RJ; Hunter WS; Moross T; Gardner HA
Prenat Diagn; 1988 Jan; 8(1):1-6. PubMed ID: 3344262
[TBL] [Abstract][Full Text] [Related]
19. [Prenatal diagnosis of two pregnancies with risk of chromosomal disorders].
Cui YX; Huang B; Shi YC; Lu HY; Xia XY; Pan LJ; Huang YF
Zhonghua Nan Ke Xue; 2007 Jul; 13(7):624-7. PubMed ID: 17725307
[TBL] [Abstract][Full Text] [Related]
20. Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at risk.
Deybach JC; Grandchamp B; Grelier M; Nordmann Y; Boué J; Boué A; de Berrianger P
Hum Genet; 1980 Feb; 53(2):217-21. PubMed ID: 7358389
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
