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3. Guide to human chromosome defects. Redding A; Hirshhorn K Birth Defects Orig Artic Ser; 1970 May; 6(1):91-106. PubMed ID: 5522728 [No Abstract] [Full Text] [Related]
4. One role for genetics in ophthalmology. Renwick JH Trans Ophthalmol Soc U K (1962); 1970; 90():111-5. PubMed ID: 5283397 [No Abstract] [Full Text] [Related]
5. [Cytogenetic studies in children with visual disorders]. Muşeţeanu P; Garoiu M; Duca-Marinescu D; Carangiu M; Friciu E; Ionescu B; Maximilian C Stud Cercet Endocrinol; 1972; 23(5):333-5. PubMed ID: 4219458 [No Abstract] [Full Text] [Related]
7. [Pediatric ophthalmology, chromosomes and heredity]. Kobayashi M Ganka; 1968 Nov; 10(11):783-9. PubMed ID: 5752351 [No Abstract] [Full Text] [Related]
8. Recent results of human cytogenetics. Clinical significance of chromosomal studies. Fleischmann T Ther Hung; 1969; 17(1):3-11. PubMed ID: 4898517 [No Abstract] [Full Text] [Related]
9. Application of new technics of chromosome identification to cytogenetic problems. Borgaonkar DS Birth Defects Orig Artic Ser; 1973 Jan; 9(1):171-82. PubMed ID: 4120145 [No Abstract] [Full Text] [Related]
10. Recent advances in cytogenetics and their relevance to medicine. Robinson JA Proc R Soc Med; 1976 Jan; 69(1):33-8. PubMed ID: 1064884 [No Abstract] [Full Text] [Related]
12. [Heredity in eye diseases. II. Foundations of ophthalmological genetics (author's transl)]. Skubiszewska T Klin Oczna; 1979 Apr; 81(4):301-4. PubMed ID: 108459 [No Abstract] [Full Text] [Related]
13. [Cytogenetic study of a mother and her son presenting the same ocular malformation]. Koulischer L; Zanen J Bull Soc Belge Ophtalmol; 1964; 138():602-11. PubMed ID: 5875584 [No Abstract] [Full Text] [Related]
14. Multiple chromosome aberrations: XO-XY-XYY mosaicism and a translocation in the same family. Ferrier PE; Ferrier SA; Schärer KO; Genton N; Hedinger C; Klein D Helv Paediatr Acta; 1967 Dec; 22(6):516-28. PubMed ID: 5592961 [No Abstract] [Full Text] [Related]
15. [Genetic study of a family presenting the combination of a chromosomal translocation and universal albinism]. André MJ; Baron A; Catros A; Dejour ; Kardjiev L; Tusques J Bull Mem Soc Fr Ophtalmol; 1972; 85(0):112-9. PubMed ID: 4671773 [No Abstract] [Full Text] [Related]
17. [Choroideremia (progressive chorio-retinal degeneration)]. François J; de Brabandere J; Stockmans L Bull Soc Belge Ophtalmol; 1967; 146():384-400. PubMed ID: 5311122 [No Abstract] [Full Text] [Related]
18. [Importance of the identification of the Q and G bands in human cytogenetics]. Vianello MG; Bonioli E Minerva Pediatr; 1974 Mar; 26(10):514-24. PubMed ID: 4827605 [No Abstract] [Full Text] [Related]
19. Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms. Eriksson B; Fraccaro M; Hultén M; Lindsten J; Thorén C; Tiepolo L Ann Genet; 1971 Dec; 14(4):281-90. PubMed ID: 5316133 [No Abstract] [Full Text] [Related]
20. The importance of chromosomal studies in ophthalmology. Weleber RG; Magenis RE Int Ophthalmol Clin; 1984; 24(1):15-38. PubMed ID: 6443568 [No Abstract] [Full Text] [Related] [Next] [New Search]