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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 7634541)

  • 1. Clinical and molecular genetic findings in five patients with Miller-Dieker syndrome.
    Köhler A; Hain J; Müller U
    Clin Genet; 1995 Mar; 47(3):161-4. PubMed ID: 7634541
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Miller-Dieker syndrome and trisomy 5p in a child carrying a derivative chromosome with a microdeletion in 17p13.3 telomeric to the LIS1 and the D17S379 loci.
    Mutchinick OM; Shaffer LG; Kashork CD; Cervantes EI
    Am J Med Genet; 1999 Jul; 85(2):99-104. PubMed ID: 10406660
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Miller-Dieker syndrome. Detection of a cryptic chromosome translocation using in situ hybridization in a family with multiple affected offspring.
    Alvarado M; Bass HN; Caldwell S; Jamehdor M; Miller AA; Jacob P
    Am J Dis Child; 1993 Dec; 147(12):1291-4. PubMed ID: 8249946
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Miller-Dieker syndrome due to maternal cryptic translocation t(10;17) (q26.3;p13.3).
    Masuno M; Imaizumi K; Nakamura M; Matsui K; Goto A; Kuroki Y
    Am J Med Genet; 1995 Dec; 59(4):441-3. PubMed ID: 8585563
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Acute lymphoblastic leukemia in a patient with Miller-Dieker syndrome.
    Czuchlewski DR; Andrews J; Madden R; Clericuzio CL; Zhang QY
    J Pediatr Hematol Oncol; 2008 Nov; 30(11):865-8. PubMed ID: 18989166
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment.
    Nagamani SC; Zhang F; Shchelochkov OA; Bi W; Ou Z; Scaglia F; Probst FJ; Shinawi M; Eng C; Hunter JV; Sparagana S; Lagoe E; Fong CT; Pearson M; Doco-Fenzy M; Landais E; Mozelle M; Chinault AC; Patel A; Bacino CA; Sahoo T; Kang SH; Cheung SW; Lupski JR; Stankiewicz P
    J Med Genet; 2009 Dec; 46(12):825-33. PubMed ID: 19584063
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal and postnatal investigation of a case with Miller-Dieker syndrome due to a familial cryptic translocation t(17;20) (p13.3;q13.3) detected by fluorescence in situ hybridization.
    van Zelderen-Bhola SL; Breslau-Siderius EJ; Beverstock GC; Stolte-Dijkstra I; de Vries LS; Stoutenbeek P; de Pater JM
    Prenat Diagn; 1997 Feb; 17(2):173-9. PubMed ID: 9061768
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. A case of Miller-Dieker syndrome in a family with neurofibromatosis type I.
    King A; Upadhyaya M; Penney C; Doshi R
    Acta Neuropathol; 2000 Apr; 99(4):425-7. PubMed ID: 10787042
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Miller-Dieker syndrome resulting from rearrangement of a familial chromosome 17 inversion detected by fluorescence in situ hybridisation.
    Kingston HM; Ledbetter DH; Tomlin PI; Gaunt KL
    J Med Genet; 1996 Jan; 33(1):69-72. PubMed ID: 8825053
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Familial Miller-Dieker syndrome and (15;17) chromosome translocation].
    Goutières F; Aicardi J; Rethore MO; Prieur M; Lejeune J
    Arch Fr Pediatr; 1987; 44(7):501-4. PubMed ID: 3426372
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.