236 related articles for article (PubMed ID: 2477654)
41. Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qter.
Al-Awadi SA; Teebi AS; Sundareshan TS
Ann Genet; 1985; 28(3):181-4. PubMed ID: 3879154
[TBL] [Abstract][Full Text] [Related]
42. Complex chromosome rearrangements and congenital anomalies.
Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
[TBL] [Abstract][Full Text] [Related]
43. Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).
D'Alessandro E; Ligas C; Lo Re ML; Marcanio MP; Gentile T; Del Porto G
J Med Genet; 1994 May; 31(5):413-5. PubMed ID: 8064823
[TBL] [Abstract][Full Text] [Related]
44. [Clinical features and genetic analysis of two cases with 16p13.3 microdeletion and 19q13.4 microduplication derived from familial cryptic balanced translocation].
Xu H; Ji X; Ni L; Zhu Y; Chen Y; Xiao B
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):490-3. PubMed ID: 27455004
[TBL] [Abstract][Full Text] [Related]
45. Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XY.
Kristoffersson U; Lagergren J; Heim S; Mandahl N
Clin Genet; 1988 Sep; 34(3):201-3. PubMed ID: 3180507
[TBL] [Abstract][Full Text] [Related]
46. Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report.
Wu D; Zhang H; Hou Q; Wang H; Wang T; Liao S
Mol Med Rep; 2017 Nov; 16(5):6222-6227. PubMed ID: 28901405
[TBL] [Abstract][Full Text] [Related]
47. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
Riegel M; Baumer A; Jamar M; Delbecque K; Herens C; Verloes A; Schinzel A
Hum Genet; 2001 Sep; 109(3):286-94. PubMed ID: 11702209
[TBL] [Abstract][Full Text] [Related]
48. [Terminal 1q deletion by translocation t(1;20)pat, confirmed by in situ hybridization].
López-Ginés C; Gil-Benso R; Gregori-Romero MA; Paredes-Cencillo C; Castelló-Pomares M; Llombart-Bosch A
An Esp Pediatr; 1998 Mar; 48(3):309-11. PubMed ID: 9608096
[No Abstract] [Full Text] [Related]
49. Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation.
Fried K; Tieder M; Beer S; Rosenblatt M; Krespin HI
J Med Genet; 1977 Feb; 14(1):68-72. PubMed ID: 839506
[TBL] [Abstract][Full Text] [Related]
50. [Subtelomeric aberration as a cause of severe somatic and psychomotor retardation in a child with dysmorphic features and CNS defects].
Kutkowska-Kaźmierczak A; Obersztyn E; Helias-Rodzewicz Z; Bocian E; Mazurczak T
Med Wieku Rozwoj; 2004; 8(4 Pt 1):949-62. PubMed ID: 15951614
[TBL] [Abstract][Full Text] [Related]
51. Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution banding.
Hersh JH; Dale KS; Gerald PS; Yen FF; Weisskopf B; Dinno ND
Am J Dis Child; 1985 Jan; 139(1):81-4. PubMed ID: 3969990
[TBL] [Abstract][Full Text] [Related]
52. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
[TBL] [Abstract][Full Text] [Related]
53. A rare unbalanced translocation 1;18 in a child with epilepsy, mild dysmorphology and mental retardation.
Vecchio D; Salzano E; Vecchio A; Roccella M
Minerva Pediatr; 2012 Jun; 64(3):365-7. PubMed ID: 22555332
[TBL] [Abstract][Full Text] [Related]
54. Alpha-thalassemia/mental retardation syndrome in a 45,X male.
Kellermayer R; Czakó M; Kiss-László Z; Gyuris P; Kozári A; Melegh B; Kosztolányi G
Am J Med Genet A; 2005 Feb; 132A(4):431-3. PubMed ID: 15633163
[TBL] [Abstract][Full Text] [Related]
55. A cytogenetic study of nonpolymalformed patients with mental retardation of clinically undefined etiology: application of a high resolution banding technique.
Kikkawa K; Narahara K; Kimoto H
Acta Med Okayama; 1989 Apr; 43(2):105-14. PubMed ID: 2728904
[TBL] [Abstract][Full Text] [Related]
56. High resolution banding analysis of the involvement of strain BALB/c- and AKR-derived chromosomes No. 15 in plasmacytoma-specific translocations.
Wiener F; Babonits M; Bregula U; Klein G; Léonard A; Wax JS; Potter M
J Exp Med; 1984 Jan; 159(1):276-91. PubMed ID: 6607313
[TBL] [Abstract][Full Text] [Related]
57. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
Fryns JP; Kleczkowska A; Kenis H
Ann Genet; 1984; 27(1):62-4. PubMed ID: 6609678
[TBL] [Abstract][Full Text] [Related]
58. Familial complex chromosomal rearrangement resulting in a recombinant chromosome.
Berend SA; Bodamer OA; Shapira SK; Shaffer LG; Bacino CA
Am J Med Genet; 2002 May; 109(4):311-7. PubMed ID: 11992486
[TBL] [Abstract][Full Text] [Related]
59. Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).
Plomp AS; Engelen JJ; Albrechts JC; de Die-Smulders CE; Hamers AJ
J Med Genet; 1998 Jul; 35(7):604-8. PubMed ID: 9678708
[TBL] [Abstract][Full Text] [Related]
60. Molecular-cytogenetic detection of a deletion of 1p36.3.
Giraudeau F; Aubert D; Young I; Horsley S; Knight S; Kearney L; Vergnaud G; Flint J
J Med Genet; 1997 Apr; 34(4):314-7. PubMed ID: 9138156
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
