These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
148 related articles for article (PubMed ID: 1879837)
1. Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13. De Rijk-van Andel JF; Catsman-Berrevoets CE; Halley DJ; Wesby-van Swaay E; Niermeijer MF; Oostra BA Hum Genet; 1991 Aug; 87(4):509-10. PubMed ID: 1879837 [TBL] [Abstract][Full Text] [Related]
2. DNA analysis in patients with lissencephaly type I and other cortical dysplasias. Oostra BA; de Rijk-van Andel JF; Eussen HJ; van Hemel JO; Halley DJ; Niermeijer MF Am J Med Genet; 1991 Sep; 40(3):383-6. PubMed ID: 1951447 [TBL] [Abstract][Full Text] [Related]
3. Submicroscopic deletions of 17p13.3 in type 1 Lissencephaly. Mantel A; Leonard C; Husson B; Miladi N; Tardieu M; Landrieu P Hum Genet; 1994 Jul; 94(1):95-6. PubMed ID: 8034303 [TBL] [Abstract][Full Text] [Related]
4. Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly. Ledbetter SA; Kuwano A; Dobyns WB; Ledbetter DH Am J Hum Genet; 1992 Jan; 50(1):182-9. PubMed ID: 1346078 [TBL] [Abstract][Full Text] [Related]
5. Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. Dobyns WB; Reiner O; Carrozzo R; Ledbetter DH JAMA; 1993 Dec; 270(23):2838-42. PubMed ID: 7907669 [TBL] [Abstract][Full Text] [Related]
6. Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome. vanTuinen P; Dobyns WB; Rich DC; Summers KM; Robinson TJ; Nakamura Y; Ledbetter DH Am J Hum Genet; 1988 Nov; 43(5):587-96. PubMed ID: 3189330 [TBL] [Abstract][Full Text] [Related]
7. Miller-Dieker syndrome with microdeletion of chromosome 17p13.3: report of one case. Huang HC; Bautista SL; Chen BS; Chang KP; Chen YJ; Wuu SW Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(6):472-6. PubMed ID: 9473821 [TBL] [Abstract][Full Text] [Related]
8. Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region. Ledbetter DH; Ledbetter SA; vanTuinen P; Summers KM; Robinson TJ; Nakamura Y; Wolff R; White R; Barker DF; Wallace MR Proc Natl Acad Sci U S A; 1989 Jul; 86(13):5136-40. PubMed ID: 2740347 [TBL] [Abstract][Full Text] [Related]
9. Localization of the Miller-Dieker critical region is proximal to locus D17S34 (p144D6) in 17p13.3. Schwartz CE; Sauer SM; Brown AM; Divelbiss JE; Patil SR Genomics; 1990 Aug; 7(4):621-4. PubMed ID: 2387588 [TBL] [Abstract][Full Text] [Related]
10. A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3. Chong SS; Pack SD; Roschke AV; Tanigami A; Carrozzo R; Smith AC; Dobyns WB; Ledbetter DH Hum Mol Genet; 1997 Feb; 6(2):147-55. PubMed ID: 9063734 [TBL] [Abstract][Full Text] [Related]
11. Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3. Cardoso C; Leventer RJ; Ward HL; Toyo-Oka K; Chung J; Gross A; Martin CL; Allanson J; Pilz DT; Olney AH; Mutchinick OM; Hirotsune S; Wynshaw-Boris A; Dobyns WB; Ledbetter DH Am J Hum Genet; 2003 Apr; 72(4):918-30. PubMed ID: 12621583 [TBL] [Abstract][Full Text] [Related]
12. Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction. Batanian JR; Ledbetter SA; Wolff RK; Nakamura Y; White R; Dobyns WB; Ledbetter DH Hum Genet; 1990 Oct; 85(5):555-9. PubMed ID: 2227942 [TBL] [Abstract][Full Text] [Related]
13. Isolated lissencephaly sequence with balanced chromosome translocation involving 17p13.3. Honda A; Ono J; Kurahashi H; Mano T; Imai K; Okada S Brain Dev; 1998 Apr; 20(3):190-2. PubMed ID: 9628198 [TBL] [Abstract][Full Text] [Related]
14. Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization. Kuwano A; Ledbetter SA; Dobyns WB; Emanuel BS; Ledbetter DH Am J Hum Genet; 1991 Oct; 49(4):707-14. PubMed ID: 1897521 [TBL] [Abstract][Full Text] [Related]
15. Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome. Schwartz CE; Johnson JP; Holycross B; Mandeville TM; Sears TS; Graul EA; Carey JC; Schroer RJ; Phelan MC; Szollar J Am J Hum Genet; 1988 Nov; 43(5):597-604. PubMed ID: 2903661 [TBL] [Abstract][Full Text] [Related]
16. Miller-Dieker syndrome with der(17)t(12;17)(q24.33;p13.3)pat presenting with a potential risk of mis-identification as a de novo submicroscopic deletion of 17p13.3. Kim YJ; Byun SY; Jo SA; Shin YB; Cho EH; Lee EY; Hwang SH Korean J Lab Med; 2011 Jan; 31(1):49-53. PubMed ID: 21239872 [TBL] [Abstract][Full Text] [Related]
17. [A case of Miller-Dieker syndrome associated with satellite on chromosome 17p]. Obara Y; Koseki N; Fujiwara J; Kikuchi M; Miura T; Funato T; Kaku M Rinsho Byori; 2001 Feb; 49(2):189-92. PubMed ID: 11307315 [TBL] [Abstract][Full Text] [Related]
18. Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphism. Pilz DT; Dalton A; Long A; Jaspan T; Maltby EL; Quarrell OW J Med Genet; 1995 Apr; 32(4):275-8. PubMed ID: 7643355 [TBL] [Abstract][Full Text] [Related]
19. Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3. Ledbetter SA; Wallace MR; Collins FS; Ledbetter DH Genomics; 1990 Jun; 7(2):264-9. PubMed ID: 2347590 [TBL] [Abstract][Full Text] [Related]