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.
141 related articles for article (PubMed ID: 1576754)
41. The chromosome 2 distal short arm trisomy syndrome. Cassidy SB; Heller RM; Chazen EM; Engel E J Pediatr; 1977 Dec; 91(6):934-8. PubMed ID: 925823 [TBL] [Abstract][Full Text] [Related]
42. Pericentric inversion of chromosome 7 (inv(7) (p22q11.2)) and ring chromosome 8 (r(8) (p23q24.3)) in a girl with minor anomalies. Verma RS; Conte RA; Pitter JH; Luke S J Med Genet; 1992 Jan; 29(1):66-7. PubMed ID: 1552550 [TBL] [Abstract][Full Text] [Related]
43. De novo ring chromosome 3: a new case with a mild phenotype. McKinley M; Colley A; Sinclair P; Donnai D; Andrews T J Med Genet; 1991 Aug; 28(8):536-8. PubMed ID: 1920370 [TBL] [Abstract][Full Text] [Related]
44. Ring chromosome 15 - cytogenetics and mapping arrays: a case report and review of the literature. Paz-Y-Miño C; Guevara-Aguirre J; Paz-Y-Miño A; Velarde F; Armendáriz-Castillo I; Yumiceba V; Hernández JM; García JL; Leone PE J Med Case Rep; 2018 Nov; 12(1):340. PubMed ID: 30442194 [TBL] [Abstract][Full Text] [Related]
45. Good growth response to growth hormone treatment in the ring chromosome 15 syndrome. Nuutinen M; Kouvalainen K; Knip M J Med Genet; 1995 Jun; 32(6):486-7. PubMed ID: 7545237 [TBL] [Abstract][Full Text] [Related]
46. Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant? Tolmie JL; Boyd E; Batstone P; Ferguson-Smith ME; al Roomi L; Connor JM Hum Genet; 1988 Oct; 80(2):197-200. PubMed ID: 3169747 [TBL] [Abstract][Full Text] [Related]
47. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report. Mattei JF; Collignon P; Ayme S; Giraud F Clin Genet; 1983 Jan; 23(1):70-4. PubMed ID: 6682021 [No Abstract] [Full Text] [Related]
48. [A case of mosaic ring chromosome 4 with subtelomeric 4p deletion]. Kim JH; Oh PS; Na HY; Kim SH; Cho HC Korean J Lab Med; 2009 Feb; 29(1):77-81. PubMed ID: 19262083 [TBL] [Abstract][Full Text] [Related]
49. Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome. Tamura T; Tohma T; Ohta T; Soejima H; Harada N; Abe K; Niikawa N Clin Dysmorphol; 1993 Apr; 2(2):106-13. PubMed ID: 7506614 [TBL] [Abstract][Full Text] [Related]
50. Inherited ring chromosome 8 without loss of subtelomeric sequences. Le Caignec C; Boceno M; Jacquemont S; Nguyen The Tich S; Rival JM; David A Ann Genet; 2004; 47(3):289-96. PubMed ID: 15337475 [TBL] [Abstract][Full Text] [Related]
51. A Novel 23.1 Mb Interstitial Deletion Involving 7q22.3q32.1 in a Girl with Short Stature, Motor Delay, and Craniofacial Dysmorphism. Del Refugio Rivera-Vega M; Gómez-Del Angel LA; Valdes-Miranda JM; Pérez-Cabrera A; Gonzalez-Huerta LM; Toral-López J; Cuevas-Covarrubias S Cytogenet Genome Res; 2015; 145(1):1-5. PubMed ID: 25870946 [TBL] [Abstract][Full Text] [Related]
52. Mixed sclerosing bone dysplasia, small stature, seizure disorder, and mental retardation: a syndrome? Jurenka SB; Van Allen MI Am J Med Genet; 1995 May; 57(1):6-9. PubMed ID: 7645600 [TBL] [Abstract][Full Text] [Related]
53. Evidence for a new microdeletion syndrome in 15q21. Liehr T; Starke H; Heller A; Weise A; Beensen V; Senger G; Kittner G; Prechtel M; Claussen U; Seidel J Int J Mol Med; 2003 May; 11(5):575-7. PubMed ID: 12684692 [TBL] [Abstract][Full Text] [Related]
54. A case of ring chromosome 15 accompanied by almost normal intelligence. Kitatani M; Takahashi H; Ozaki M; Okino E; Maruoka T Hum Genet; 1990 Jun; 85(1):138-9. PubMed ID: 2358298 [TBL] [Abstract][Full Text] [Related]
55. 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]
56. Ring chromosome 15 syndrome in an adult female. Matsuishi T; Yamada Y; Endo K; Sakai H; Fukushima Y J Intellect Disabil Res; 1996 Oct; 40 ( Pt 5)():478-80. PubMed ID: 8906535 [TBL] [Abstract][Full Text] [Related]
57. Duplication of 14q11.2 associates with short stature and mild mental retardation: a putative relation with quantitative trait loci. Monfort S; Blesa D; Roselló M; Orellana C; Oltra S; Cigudosa JC; Martínez F Am J Med Genet A; 2007 Feb; 143(4):382-4. PubMed ID: 17230491 [No Abstract] [Full Text] [Related]
58. Ring chromosome 11. A case report and review of the literature. Palka G; Verrotti A; Peca S; Mosca L; Lombardo G; Verrotti M; Morgese G Ann Genet; 1986; 29(1):55-8. PubMed ID: 3487279 [TBL] [Abstract][Full Text] [Related]
59. Flecked retina associated with ring 17 chromosome. Charles SJ; Moore AT; Davison BC; Dyson HM; Willatt L Br J Ophthalmol; 1991 Feb; 75(2):125-7. PubMed ID: 1995042 [TBL] [Abstract][Full Text] [Related]
60. Radio-ulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation. Tsukahara M; Matsuo K; Furukawa S Am J Med Genet; 1995 Aug; 58(2):159-60. PubMed ID: 8533809 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]