156 related articles for article (PubMed ID: 4265215)
1. Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.
Warren RJ; Rimoin DL; Summitt RL
Am J Hum Genet; 1973 Jan; 25(1):77-81. PubMed ID: 4265215
[No Abstract] [Full Text] [Related]
2. Ring-G chromosome, a new G-deletion syndrome?
Weleber RG; Hecht F; Giblett ER
Am J Dis Child; 1968 Apr; 115(4):489-93. PubMed ID: 4296014
[No Abstract] [Full Text] [Related]
3. Ring chromosome 7 with variable phenotypic expression.
Zackai EH; Breg WR
Cytogenet Cell Genet; 1973; 12(1):40-8. PubMed ID: 4145271
[No Abstract] [Full Text] [Related]
4. G-deletion syndrome II.
Chauvel PJ; Schindeler JD; Warren RJ
Humangenetik; 1972; 14(2):164-6. PubMed ID: 5026850
[No Abstract] [Full Text] [Related]
5. Partial trisomy 21.
Aula P; Leisti J; von Koskull H
Clin Genet; 1973; 4(3):241-51. PubMed ID: 4128808
[No Abstract] [Full Text] [Related]
6. A ring-20 chromosome.
Atkins L; Miller WL; Salam M
J Med Genet; 1972 Sep; 9(3):377-80. PubMed ID: 4627939
[No Abstract] [Full Text] [Related]
7. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
Gustavson KH; Hitrec V; Santesson B
Clin Genet; 1972; 3(2):135-46. PubMed ID: 5054315
[No Abstract] [Full Text] [Related]
8. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.
Rosenthal IM; Krmpotic E; Bocian M; Szego K
Clin Genet; 1973 Jun; 4(6):507-16. PubMed ID: 4787842
[No Abstract] [Full Text] [Related]
9. Distinction between extra G-like chromosomes by quinacrine mustard fluorescence analysis.
Caspersson T; Hultén M; Lindsten J; Zech L
Exp Cell Res; 1970 Nov; 63(1):240-3. PubMed ID: 4250490
[No Abstract] [Full Text] [Related]
10. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
del Solar C; Uchida IA
J Pediatr; 1974 Apr; 84(4):534-8. PubMed ID: 4134885
[No Abstract] [Full Text] [Related]
11. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
Crandall BF; Weber F; Muller HM; Burwell JK
Clin Genet; 1972; 3(4):264-70. PubMed ID: 5054320
[No Abstract] [Full Text] [Related]
12. An 18p21q translocation in a patient with presumptive "monosomy G".
Cohen MM; Putnam TI
Am J Dis Child; 1972 Dec; 124(6):908-10. PubMed ID: 4639227
[No Abstract] [Full Text] [Related]
13. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
Miller JQ
Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
[No Abstract] [Full Text] [Related]
14. Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) and microcephaly.
Ishikiriyama S; Goto M
Am J Med Genet; 1994 Aug; 52(2):245. PubMed ID: 7802022
[No Abstract] [Full Text] [Related]
15. G-group ring chromosome in a mentally subnormal girl.
Richards BW; Rundle AT; Hatton WM; Stewart A
J Ment Defic Res; 1971 Mar; 15(1):61-72. PubMed ID: 4253116
[No Abstract] [Full Text] [Related]
16. Banding identification of chromosomal abnormalities in four patients: ring (6), translocation (2q-;15q+), translocation (21q;21q) and deletion (22q-).
Wurster-Hill DH; Hoefnagel D
J Ment Defic Res; 1975 Jun; 19(2):145-50. PubMed ID: 127842
[TBL] [Abstract][Full Text] [Related]
17. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2.
Pallotta R
J Med Genet; 1991 May; 28(5):342-4. PubMed ID: 1865474
[TBL] [Abstract][Full Text] [Related]
18. Chromosomes and mental retardation.
Baraitser M
Psychol Med; 1986 Aug; 16(3):495-7. PubMed ID: 2945219
[No Abstract] [Full Text] [Related]
19. New techniques in the study of human chromosomes: methods and applications.
Dutrillaux B; Lejeune J
Adv Hum Genet; 1975; 5():119-56. PubMed ID: 48327
[No Abstract] [Full Text] [Related]
20. Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.
Mikkelsen M
Humangenetik; 1971; 12(1):67-73. PubMed ID: 4104181
[No Abstract] [Full Text] [Related]
[Next] [New Search]
