104 related articles for article (PubMed ID: 21664500)
21. Prospective screening of patients with unexplained mental retardation using subtelomeric MLPA strongly increases the detection rate of cryptic unbalanced chromosomal rearrangements.
Stegmann AP; Jonker LM; Engelen JJ
Eur J Med Genet; 2008; 51(2):93-105. PubMed ID: 18032123
[TBL] [Abstract][Full Text] [Related]
22. Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH.
Joyce CA; Dennis NR; Cooper S; Browne CE
Hum Genet; 2001 Oct; 109(4):440-51. PubMed ID: 11702226
[TBL] [Abstract][Full Text] [Related]
23. Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.
Pettenati MJ; Teot LA; Smith C; Hayworth R; Thomas IT; Veille JC; Rao PN
Am J Med Genet; 1993 Feb; 45(3):365-9. PubMed ID: 8434625
[TBL] [Abstract][Full Text] [Related]
24. [Autosomal anomalies in a specially selected group of children with mental retardation without signs of Down's syndrome].
Bliumina MG; Demintseva VS; Podugol'nikova OA
Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(3):55-8. PubMed ID: 7080777
[TBL] [Abstract][Full Text] [Related]
25. Characterization of a Rare Mosaicism in Autosomal Translocation of t(5;21) Using Conventional Cytogenetics and FISH Methods.
Omori Sarabi S; Karimzad Hagh J; Behrend C; Mohseni SB; Ansari Dezfouli M; Rashidi SK; Omrani MD
Iran Biomed J; 2020 Jan; 24(1):60-3. PubMed ID: 31301695
[TBL] [Abstract][Full Text] [Related]
26. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC
Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
[TBL] [Abstract][Full Text] [Related]
27. 4p trisomy syndrome: report of 4 additional cases and segregation analysis of 21 families with different translocations.
Crane J; Sujansky E; Smith A
Am J Med Genet; 1979; 4(3):219-29. PubMed ID: 517577
[TBL] [Abstract][Full Text] [Related]
28. [A clinical and cytogenetic investigation carried out in a special institution for mentally retarded patients: preliminary results concerning 82 cases of oligophrenia (author's transl)].
Mounoud RL; Klein D; Bettschart W; Cabrol C
J Genet Hum; 1976 Dec; 24(4):297-335. PubMed ID: 1022853
[TBL] [Abstract][Full Text] [Related]
29. De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation.
Chaganti RS; Morillo-Cucci G; Friis L; Degnan M; German J
Ann Genet; 1976 Mar; 19(1):43-8. PubMed ID: 1084121
[TBL] [Abstract][Full Text] [Related]
30. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
31. Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries.
Jehee FS; Takamori JT; Medeiros PF; Pordeus AC; Latini FR; Bertola DR; Kim CA; Passos-Bueno MR
Eur J Med Genet; 2011; 54(4):e425-32. PubMed ID: 21457803
[TBL] [Abstract][Full Text] [Related]
32. [Translocation (13; 18) (q22; p 11) and prenatal diagnosis (author's transl)].
Wagenbichler P; Golob E; Schnedl W
Wien Klin Wochenschr; 1976 Oct; 88(19):646-8. PubMed ID: 983074
[TBL] [Abstract][Full Text] [Related]
33. A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.
Talseth-Palmer BA; Bowden NA; Meldrum C; Nicholl J; Thompson E; Friend K; Liebelt J; Bratkovic D; Haan E; Yu S; Scott RJ
Cytogenet Genome Res; 2009; 124(1):94-101. PubMed ID: 19372674
[TBL] [Abstract][Full Text] [Related]
34. Chromosome studies of 500 couples with two or more abortions.
Sachs ES; Jahoda MG; Van Hemel JO; Hoogeboom AJ; Sandkuyl LA
Obstet Gynecol; 1985 Mar; 65(3):375-8. PubMed ID: 3974963
[TBL] [Abstract][Full Text] [Related]
35. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
[TBL] [Abstract][Full Text] [Related]
36. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
Roos A; Rudnik-Schöneborn S; Eggermann K; Eggermann T; Senderek J; Schwanitz G; Zerres K; Schüler HM
Eur J Med Genet; 2006; 49(6):505-10. PubMed ID: 16905374
[TBL] [Abstract][Full Text] [Related]
37. "Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents.
Wenger SL; Steele MW; Boone LY; Lenkey SG; Cummins JH; Chen XQ
Am J Med Genet; 1995 Jan; 55(1):47-52. PubMed ID: 7702096
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT
Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871
[TBL] [Abstract][Full Text] [Related]
40. Successful pregnancy after preimplantation genetic diagnosis for carrier of t(2;7)(p11.2;q22) with high rates of unbalanced sperm and embryos: a case report.
Wiland E; Hobel CJ; Hill D; Kurpisz M
Prenat Diagn; 2008 Jan; 28(1):36-41. PubMed ID: 18186141
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
