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3. [CHROMOSOME STUDIES IN CONGENITAL DEFECTS OF THE HEART AND GREAT VESSELS]. KAINDL F; SCHOBER B; ROTHENBUCHER G Wien Z Inn Med; 1965 Mar; 46():105-8. PubMed ID: 14305865 [No Abstract] [Full Text] [Related]
4. [Chromosome aberrations in ophthalmology]. François J; Berger R; Saraux H Bull Mem Soc Fr Ophtalmol; 1972; 85(0):1-37. PubMed ID: 4671737 [No Abstract] [Full Text] [Related]
5. [BLOOD GROUPS AND HUMAN GENETICS]. RUFFIE J Nouv Rev Fr Hematol; 1965; 5():175-90. PubMed ID: 14280631 [No Abstract] [Full Text] [Related]
6. A statistical study of the brachial indices of chromosomes 1,2 and 3, and of an heterozygous abnormality of chromosomes 1. Galperin H Humangenetik; 1966; 2(4):387-91. PubMed ID: 5959953 [No Abstract] [Full Text] [Related]
7. Report of the second international workshop on human chromosome 10 mapping 1997. Meitinger T; Scharfe C; Call K; Moschonas N Cytogenet Cell Genet; 1997; 78(3-4):184-94. PubMed ID: 9465886 [No Abstract] [Full Text] [Related]
8. The chromosome, its anatomy, and its aberrations. Yang-Feng TL Res Publ Assoc Res Nerv Ment Dis; 1991; 69():19-38. PubMed ID: 2003160 [No Abstract] [Full Text] [Related]
9. Report and abstracts of the third international workshop on human chromosome 1 mapping 1997. Vance JM; Matise TC; Wooster R; Schutte BC; Bruns GA; van Roy N; Brodeur GM; Tao YX; Gregory S; Weith A; Vaudin M; White P Cytogenet Cell Genet; 1997; 78(3-4):154-82. PubMed ID: 9465885 [No Abstract] [Full Text] [Related]
10. [Progress in the studies of chromosomes in children with multiple developmental anomalies]. Gajewska-Obel E Pediatr Pol; 1980 Jan; 55(1):125-31. PubMed ID: 6154280 [No Abstract] [Full Text] [Related]
11. The chromosomes of man--clinical and biologic significance. A review. Yunis JJ; Chandler ME Am J Pathol; 1977 Aug; 88(2):466-96. PubMed ID: 69405 [No Abstract] [Full Text] [Related]
12. [The chromosome in chromosome aberrations and hereditary diseases]. CARTIER F Fr Med; 1961; 24():369-78. PubMed ID: 13876978 [No Abstract] [Full Text] [Related]
13. 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]
16. Mapping of the gene for multiple endocrine neoplasia type I to chromosome 11q13. Nordenskjöld M; Larsson C; Oberg K; Nakamura Y Pathol Biol (Paris); 1989 Nov; 37(9):951. PubMed ID: 2575240 [No Abstract] [Full Text] [Related]
17. Chromosome identification. Hirschhorn K Annu Rev Med; 1973; 24():67-74. PubMed ID: 4122896 [No Abstract] [Full Text] [Related]