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.
2. [The normal karyotype and the karyotype in the principal autosome and gonosome anomalies]. Le Marec B Cah Med; 1971 Jun; 12(10):817-24. PubMed ID: 5112586 [No Abstract] [Full Text] [Related]
3. A diagnostic survey of infants referred for chromosome analysis in the neonatal period. Winter RM; Ridler MA; McKeown JA Br Med J; 1980 Oct; 281(6247):1045-7. PubMed ID: 6448659 [TBL] [Abstract][Full Text] [Related]
4. [Clinical and cytogenetic findings in a rare autosomal aberrations]. Tolksdorf M Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):308-13. PubMed ID: 5523669 [No Abstract] [Full Text] [Related]
6. Chromosomal anomalies in patients with retinoblastoma. Neetens A; Dumon J; De Smet N; Neetens I Bull Soc Belge Ophtalmol; 1982; 203():47-56. PubMed ID: 7187621 [No Abstract] [Full Text] [Related]
7. [Significance of chromosome aberrations to the pediatrician]. Stoeckenius M Monatsschr Kinderheilkd (1902); 1968 Jul; 116(7):446-8. PubMed ID: 4239142 [No Abstract] [Full Text] [Related]
8. Autosomal chromosome aberrations. A review of the clinical syndromes caused by structural chromosome aberrations, mosaic-trisomies 8 and 9, and triploidy. Schinzel A Ergeb Inn Med Kinderheilkd; 1976; 38():37-94. PubMed ID: 782877 [No Abstract] [Full Text] [Related]
9. Chromosome analysis in newborns: clinical considerations. Lee LG J Miss State Med Assoc; 1971 Jun; 12(6):297-302. PubMed ID: 5132295 [No Abstract] [Full Text] [Related]
14. Abnormal chromosome complement after normal amniocentesis result. Berry AC; Docherty Z; Bobrow M Lancet; 1992 Nov; 340(8831):1361. PubMed ID: 1360083 [No Abstract] [Full Text] [Related]
15. [Congenital ocular malformations encountered in structural and numerical chromosomal anomalies]. Chercotă G; Budău M; Olaru G Rev Chir Oncol Radiol O R L Oftalmol Stomatol Ser Oftalmol; 1989; 33(3):193-6. PubMed ID: 2532765 [TBL] [Abstract][Full Text] [Related]
16. [Chromosomal diseases in children]. Demidova IA Med Sestra; 1988 Sep; 47(9):31-4. PubMed ID: 3205133 [No Abstract] [Full Text] [Related]
17. "Cri du Chat" due to a ring-B chromosome. Rohde RA; Tompkins R Lancet; 1965 Nov; 2(7421):1075-6. PubMed ID: 4159145 [No Abstract] [Full Text] [Related]
18. A case of deletion of short arm of chromosome 8. Leisti J; Aula P Birth Defects Orig Artic Ser; 1977; 13(3B):187-94. PubMed ID: 890091 [No Abstract] [Full Text] [Related]
19. [Chromosome aberrations in fetuses and neonates]. Boczkowski K Postepy Hig Med Dosw; 1981; 34(6):479-89. PubMed ID: 7291083 [No Abstract] [Full Text] [Related]
20. Anti-mongolism. Studies in an infant with a partial monosomy of the 21 chromosome. Reisman LE; Kashara S; Chung CY; Darnell A; Hall B Lancet; 1966 Feb; 1(7434):394-7. PubMed ID: 4159779 [No Abstract] [Full Text] [Related] [Next] [New Search]