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.
4. Structural variation in human nitotic chromosomes. Leisti J Ann Acad Sci Fenn Biol; 1971; 179():1-69. PubMed ID: 4261167 [No Abstract] [Full Text] [Related]
5. [Occurrence of chromosome abnormalities in sick and healthy persons]. Pfeiffer RA; Majewski F Internist (Berl); 1971 Jan; 12(1):1-7. PubMed ID: 4925386 [No Abstract] [Full Text] [Related]
6. II. A review of clinical syndromes associated with aberrations of the autosomes. Williams JD; Summitt RL J Tenn Med Assoc; 1971 Apr; 64(4):310-7. PubMed ID: 4252589 [No Abstract] [Full Text] [Related]
10. A new recognizable syndrome associated with a chromosomal abnormality. Handmaker SD; Hall BD; Conte FA Birth Defects Orig Artic Ser; 1975; 11(5):181-9. PubMed ID: 1218211 [No Abstract] [Full Text] [Related]
11. [Chromosome aberrations in abortions]. Boué JG; Boué A; Lazar P Ann Genet; 1967 Dec; 10(4):179-87. PubMed ID: 5301690 [No Abstract] [Full Text] [Related]
12. [RV polymorphism of the chromosomes in newborn infants]. Krachunova M; Tsancheva M; Lozanova T Eksp Med Morfol; 1980; 19(3):144-8. PubMed ID: 7418645 [TBL] [Abstract][Full Text] [Related]
13. [46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child]. de Grouchy J; Lautmann F Ann Genet; 1968 Jun; 11(2):129-31. PubMed ID: 5303425 [No Abstract] [Full Text] [Related]
14. Frequency of qh+ chromosomal variants in a) radioexposed, b) Down syndrome and c) control subjects. Saccucci F; Catena Q; Dolcini F; Donati D; Magistrelli R; Valentini B; Milani-Comparetti M Boll Soc Ital Biol Sper; 1983 Aug; 59(8):1070-5. PubMed ID: 6226304 [TBL] [Abstract][Full Text] [Related]
15. [Incidence of the qh+ varients in the karyotype of subjects occupationally exposed to ionizing radiations]. Milani-Comparetti M; Catena Q; Donati D; Magistrelli R; Nataloni P; Saccucci F Boll Soc Ital Biol Sper; 1980 Mar; 56(6):549-55. PubMed ID: 7378188 [TBL] [Abstract][Full Text] [Related]
16. [Polymorphism of the C band of chromosomes in clinical patients]. Kosztolányi G Orv Hetil; 1982 Sep; 123(36):2231-4. PubMed ID: 6890197 [No Abstract] [Full Text] [Related]
17. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation]. Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734 [No Abstract] [Full Text] [Related]