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.
117 related articles for article (PubMed ID: 147507)
41. Down syndrome with unusual familial translocation (1;21). A case report. Sayee R; Thomas IM Ann Genet; 1993; 36(3):171-2. PubMed ID: 8117064 [TBL] [Abstract][Full Text] [Related]
42. [Trisomy 21 and trisomy 18 in siblings]. Girardet P; Grosset L; Juillard E Helv Paediatr Acta; 1972 Dec; 27(6):583-9. PubMed ID: 4265243 [No Abstract] [Full Text] [Related]
46. A familial tandem translocation (15;21) (q11;q22) in a case of Down's syndrome. Wahlström J; Djerg S J Ment Defic Res; 1976 Sep; 20(3):171-8. PubMed ID: 135089 [No Abstract] [Full Text] [Related]
47. [Down's syndrome in our study material]. Bujdosó G; Sziller I Morphol Igazsagugyi Orv Sz; 1977 Jul; 17(3):167-72. PubMed ID: 144867 [No Abstract] [Full Text] [Related]
48. A case of 47,XX,(21q-)+ with some stigmata of Down's syndrome and an IQ of 77. Neu RL; Voorhess ML; Gardner LI J Med Genet; 1971 Dec; 8(4):528-9. PubMed ID: 4261059 [No Abstract] [Full Text] [Related]
50. Trisomy 18 and trisomy 21 mosaicism in a Down's syndrome patient. Thomas IM; Sayee R; Shavanthi L; Sridevi H J Med Genet; 1994 May; 31(5):418-9. PubMed ID: 8064824 [TBL] [Abstract][Full Text] [Related]
51. Mitotic and meiotic chromosomes in a family with repeated miscarriages and two children with trisomy-G Down's syndrome. De la Chapelle A; Kjessler B; Johansson CJ; Saari R; Kauste O J Ment Defic Res; 1967 Jun; 11(2):69-78. PubMed ID: 4226942 [No Abstract] [Full Text] [Related]
52. Marker chromosomes in parents to children with Down's syndrome. Annerén G; Wahlström J; Tommerup N Clin Genet; 1984 Feb; 25(2):140-7. PubMed ID: 6231142 [TBL] [Abstract][Full Text] [Related]
53. [Chromosome findings in 365 patients with Down's syndrome or suspected Down's syndrome]. Engel W; Reinwein H; Müller I; Kunze G Humangenetik; 1970; 8(4):307-11. PubMed ID: 4245033 [No Abstract] [Full Text] [Related]
54. A case of 48,XXY,21+ in an infant with Down's syndrome. Neu RL; Scheuer AQ; Gardner LI J Med Genet; 1971 Dec; 8(4):533-5. PubMed ID: 4260531 [No Abstract] [Full Text] [Related]
55. Double trisomy with 48, XXX+21 karyotype in a Down's syndrome child from Jammu and Kashmir, India. Balwan WK; Kumar P; Raina TR; Gupta S J Genet; 2008 Dec; 87(3):257-9. PubMed ID: 19147910 [No Abstract] [Full Text] [Related]
56. [Unusual karyotype in a child with Down's disease]. Kristesashvili DI Pediatriia; 1985 Apr; (4):69-70. PubMed ID: 3158878 [No Abstract] [Full Text] [Related]
57. Apparent G-monosomy, G-deletion, and incomplete Down's syndrome in a single family. Schmidt R; Mundel G; Rosenblatt M; Katznelson MB J Med Genet; 1972 Dec; 9(4):457-61. PubMed ID: 4265014 [No Abstract] [Full Text] [Related]
58. [Low blood iron content in children with Down's syndrome]. Wachowicz B; Kdziora J Endokrynol Pol; 1974; 25(1):9-13. PubMed ID: 4277223 [No Abstract] [Full Text] [Related]
59. The frequency of trisomy and translocation in Down's syndrome. Wright SW; Day RW; Muller H; Weinhouse R J Pediatr; 1967 Mar; 70(3):420-4. PubMed ID: 4225160 [No Abstract] [Full Text] [Related]