571 related articles for article (PubMed ID: 9599644)
21. Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation.
Shamdeen A; Meyer S; Gottschling S; Oehl-Jaschkowitz B; Gortner L; Shamdeen MG
Klin Padiatr; 2009; 221(2):97-9. PubMed ID: 19067289
[TBL] [Abstract][Full Text] [Related]
22. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
[TBL] [Abstract][Full Text] [Related]
23. Cytogenetic abnormalities in orthopedic patients.
Cowell HR; Clark CE
Clin Orthop Relat Res; 1978 Sep; (135):4-14. PubMed ID: 152176
[TBL] [Abstract][Full Text] [Related]
24. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
25. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
[TBL] [Abstract][Full Text] [Related]
26. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
27. De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.
Curotti G; Benkhalifa M; Raybaud C; Picard F; Bellec V; Qumsiyeh MB
Genet Couns; 1999; 10(3):259-64. PubMed ID: 10546097
[TBL] [Abstract][Full Text] [Related]
28. [Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].
Nazarenko SA; Nazarenko LP; Baranova VA
Tsitol Genet; 1987; 21(6):434-7. PubMed ID: 3445362
[TBL] [Abstract][Full Text] [Related]
29. Chromosome missegregation and trisomy 21 mosaicism in Alzheimer's disease.
Geller LN; Potter H
Neurobiol Dis; 1999 Jun; 6(3):167-79. PubMed ID: 10408806
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
31. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
Gibson LH; McGrath J; Yang-Feng TL
Am J Med Genet; 1997 Feb; 68(4):417-20. PubMed ID: 9021014
[TBL] [Abstract][Full Text] [Related]
32. [An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization].
Zerova TE; Baronova EV; Gorovenko NG; Koblianskaia GN; Buzhievskaia TI; Vorsanova SG; Iurov IuB
Tsitol Genet; 1995; 29(5):41-8. PubMed ID: 8721845
[TBL] [Abstract][Full Text] [Related]
33. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A
Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600
[TBL] [Abstract][Full Text] [Related]
34. Inv dup(15) supernumerary marker chromosomes.
Webb T
J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
[No Abstract] [Full Text] [Related]
35. A case of mosaic Down's syndrome with two Robertsonian translocations.
Leal-Garza CH; Cortés-Gutiérrez EI; Ortiz-Jalomo R; García-Cavazos R
Rev Invest Clin; 1996; 48(5):385-8. PubMed ID: 8968157
[TBL] [Abstract][Full Text] [Related]
36. Cytogenetic characterization of cat eye syndrome marker chromosome.
Wenger SL; Surti U; Nwokoro NA; Steele MW
Ann Genet; 1994; 37(1):33-6. PubMed ID: 8010712
[TBL] [Abstract][Full Text] [Related]
37. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
Iourov IY; Soloviev IV; Vorsanova SG; Monakhov VV; Yurov YB
J Histochem Cytochem; 2005 Mar; 53(3):401-8. PubMed ID: 15750029
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
Mark HF; Wyandt H; Huang XL; Milunsky JM
Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
[TBL] [Abstract][Full Text] [Related]
40. Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.
Juyal RC; Kuwano A; Kondo I; Zara F; Baldini A; Patel PI
Am J Med Genet; 1996 Dec; 66(2):193-6. PubMed ID: 8958329
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
