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2. Variations of centromeric region of chromosome no. 1 and no. 9 in one family. Ku56cerov57A M; Polívková Z Humangenetik; 1974; 22(4):327-30. PubMed ID: 4426626 [No Abstract] [Full Text] [Related]
3. Inversion of 'flourescent' segment in chromosome 3: a polymorphic trait. Soudek D; Sroka H Hum Genet; 1978 Oct; 44(2):109-15. PubMed ID: 730157 [TBL] [Abstract][Full Text] [Related]
4. 1q plus variants in a normal adult population (one with a pericentric inversion). Tüür S; Käosaar M; Mikelsaar AV Humangenetik; 1974; 24(3):217-20. PubMed ID: 4140833 [No Abstract] [Full Text] [Related]
5. Longitudinal differentiation of human mitotic chromosomes. Communication II. Analysis of pericentric inversion of the first chromosome in a child with anomalous sex differentiation. Seleznev YuV ; Dzenis IG Sov Genet; 1974 Jul; 8(6):770-3. PubMed ID: 4421586 [No Abstract] [Full Text] [Related]
6. Paracentric Inversion in man: personal experience and review of the literature. Fryns JP; Van den Berghe H Hum Genet; 1980; 54(3):413-6. PubMed ID: 7399530 [No Abstract] [Full Text] [Related]
7. Malformations in a child with dup (7pter-p15.1) and del (7q36-qter) as a result of familial pericentric inversion. Ramer JC; Mowrey PN; Ladda RL Clin Genet; 1991 Jun; 39(6):442-50. PubMed ID: 1863992 [TBL] [Abstract][Full Text] [Related]
8. Giemsa banding of chromosome 1gh+ and linkage analysis. Howard PN; Stoddard GR; Goddard MW; Seely JR J Med Genet; 1975 Mar; 12(1):44-8. PubMed ID: 47395 [TBL] [Abstract][Full Text] [Related]
10. [Cytogenetic study of a case of Fanconi's syndrome with a familial pericentric inversion]. Crippa L; Ferrier S J Genet Hum; 1975 Mar; 23(1):7-16. PubMed ID: 1165481 [TBL] [Abstract][Full Text] [Related]
11. [Pericentric inversions of chromosomes 1, 9 and 16 in patients with sex chromosome anomalies]. Verlinskaia DK; Prozorova MV; Khitrikov LE Tsitol Genet; 1982; 16(1):57-60. PubMed ID: 7064223 [TBL] [Abstract][Full Text] [Related]
12. Pericentric inversion Y in a population of newborn boys. Friedrich U; Nielsen J Hereditas; 1974; 76(1):147-52. PubMed ID: 4136008 [No Abstract] [Full Text] [Related]
13. Variant chromosome 3 (inv3) in normal newborns and their parents, and in children with mental retardation. Mikelsaar AV; Ilus T; Kivi S Hum Genet; 1978 Feb; 41(1):109-13. PubMed ID: 631855 [TBL] [Abstract][Full Text] [Related]
14. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl. Jacobsen P; Mikkelsen M; Rosleff F Clin Genet; 1973; 4(5):434-41. PubMed ID: 4127395 [No Abstract] [Full Text] [Related]
15. Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7. Winsor EJ; Palmer CG; Ellis PM; Hunter JL; Ferguson-Smith MA Cytogenet Cell Genet; 1978; 20(1-6):169-84. PubMed ID: 648176 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. A child with a recombinant of chromosome 8 inherited from her carrier mother. Barnes IC; Kumar D; Bell RJ J Med Genet; 1985 Feb; 22(1):67-70. PubMed ID: 3981583 [TBL] [Abstract][Full Text] [Related]
18. Pericentric inversion of chromosome 11 in one of two similar retarded brothers. Einfeld SL; Smith A J Med Genet; 1982 Aug; 19(4):312. PubMed ID: 7120323 [No Abstract] [Full Text] [Related]
19. Abnormal chromosome complement resulting from a familial inversion of chromosome 2. Richter S; Lockwood B; Lockwood D; Allanson J J Med Genet; 1989 Nov; 26(11):725-9. PubMed ID: 2479747 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]