151 related articles for article (PubMed ID: 4115504)
1. The XYY syndrome in an adolescent male exhibiting prominent behavioral problems.
Alam MT; Deschamps R; Gaba E; Kasatiya SS; Grant WF
Clin Genet; 1972; 3(3):162-8. PubMed ID: 4115504
[No Abstract] [Full Text] [Related]
2. Quantitative studies of Y chromosomal fluorescence in human interphase nuclei.
Lamborot-Manzur M; Tishler PV; Atkins L
Clin Genet; 1972; 3(2):103-15. PubMed ID: 4115478
[No Abstract] [Full Text] [Related]
3. [Fluorescence diagnosis of sex chromosomes in the XYY syndrome].
Kowalska E; Wiśniewski L
Z Hautkr; 1974 Jul; 49(13):571-4. PubMed ID: 4138706
[No Abstract] [Full Text] [Related]
4. 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]
5. Inherited t(13q14q) in two retarded sisters.
Crandall BF; Francke U; Campbell MA; Sparkes RS
Am J Hum Genet; 1972 Jul; 24(4):416-24. PubMed ID: 5031981
[No Abstract] [Full Text] [Related]
6. An adult male with XYYY sex chromosomes.
Ridler MA; Lax R; Mitchell MJ; Shapiro A; Saldaña-Garcia P
Clin Genet; 1973; 4(1):69-77. PubMed ID: 4691557
[No Abstract] [Full Text] [Related]
7. 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]
8. A familial Y-autosome translocation in man.
Noel B; Emerit I; Luciani JM; Quack B
Clin Genet; 1971; 2(1):1-6. PubMed ID: 5111751
[No Abstract] [Full Text] [Related]
9. 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]
10. Immunoglobulin abnormality in a girl with a large chromosome 18.
Yanagisawa S
J Med Genet; 1972 Sep; 9(3):360-5. PubMed ID: 4116772
[No Abstract] [Full Text] [Related]
11. [Effect of the Y chromosome on the morphology of human F-chromatin under normal and pathological conditions].
Kulikov RI
Tsitologiia; 1977 Jul; 19(7):732-8. PubMed ID: 73242
[TBL] [Abstract][Full Text] [Related]
12. Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocation.
Fründ S; Koske-Westphal T; Fuchs-Mecke S; Passarge E
Humangenetik; 1972; 14(2):133-6. PubMed ID: 4112732
[No Abstract] [Full Text] [Related]
13. [Identification of Y-chromosome anomalies using fluorescence microscopy. Study on 2 groups of prisoners as a contribution to the XYY problem].
Hellweg-Fründ S; Koske-Westphal T; Fuchs-Mecke S; Passarge E
Dtsch Med Wochenschr; 1972 Oct; 97(43):1650-4 passim. PubMed ID: 4117258
[No Abstract] [Full Text] [Related]
14. Polymorphism of the human Y chromosomes: fluorescence microscopic studies on the sites of morphologic variation.
Tishler PV; Lamborot-Manzur M; Atkins L
Clin Genet; 1972; 3(2):116-22. PubMed ID: 4115479
[No Abstract] [Full Text] [Related]
15. An XYY baby with Prader syndrome.
Iinuma K; Tanae A; Tanaka G
Clin Genet; 1974; 6(4):323-5. PubMed ID: 4442235
[No Abstract] [Full Text] [Related]
16. Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies.
Kakati S; Sinha AK
Hum Hered; 1973 Apr; 23(4):313-30. PubMed ID: 4130026
[No Abstract] [Full Text] [Related]
17. Identification of partial 12 trisomy by quinacrine fluorescence.
Uchida IA; Lin CC
J Pediatr; 1973 Feb; 82(2):269-72. PubMed ID: 4119313
[No Abstract] [Full Text] [Related]
18. Y-specific fluorescence in peripheral blood leukocytes.
Thuline HC
J Pediatr; 1971 May; 78(5):875-6. PubMed ID: 4103343
[No Abstract] [Full Text] [Related]
19. Non-fluorescent Y-chromosome.
Bühler EM; Bühler UK; Tsuchimoto T; Stalder GR
Helv Paediatr Acta; 1974 Nov; 29(5):447-56. PubMed ID: 4141700
[No Abstract] [Full Text] [Related]
20. Conenital hypothyroidism in association with a ring chromosome 18.
Winter JS; Ahluwalia K; Ray M
J Med Genet; 1972 Mar; 9(1):122-6. PubMed ID: 5025476
[No Abstract] [Full Text] [Related]
[Next] [New Search]
