Pages that link to "Q72668345"

The following pages link to Localization of the human α-globin gene cluster to the short arm of chromosome 16 (16p12–16pter) by hybridization in situ (Q72668345):

Displaying 24 items.

• High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization (Q24614305) (← links)
• Chromosomal location of the genes encoding the leukocyte adhesion receptors LFA-1, Mac-1 and p150,95. Identification of a gene cluster involved in cell adhesion (Q24682479) (← links)
• High resolution gene mapping of the human alpha globin locus (Q33674101) (← links)
• Mapping the human alpha globin gene complex to 16p13.2----pter (Q33676507) (← links)
• Alpha-thalassaemia (Q33953611) (← links)
• The molecular genetics of human hemoglobin (Q34258836) (← links)
• Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization (Q35203563) (← links)
• The human myoglobin gene: a third dispersed globin locus in the human genome (Q35274323) (← links)
• Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization. (Q36307937) (← links)
• Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p. (Q36415470) (← links)
• Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis (Q36473258) (← links)
• Human genome structure (Q39837424) (← links)
• Localisation of the human N-ras oncogene to chromosome 1cen - p21 by in situ hybridisation (Q41466847) (← links)
• Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16. (Q41764243) (← links)
• The chromosome breakpoint at 14q32 in an ataxia telangiectasia t(14;14) T cell clone is different from the 14q32 breakpoint in Burkitts and an inv(14) T cell lymphoma (Q58420434) (← links)
• A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 (Q59066375) (← links)
• Chromosomal localization of ceruloplasmin and transferrin genes in laboratory rats, mice and in man by hybridization with specific DNA probes (Q68670916) (← links)
• A subpopulation of t(2;14)(p11;q32) cells in ataxia telangiectasia B lymphocytes (Q68803668) (← links)
• Growth of large chromosomally abnormal T cell clones in ataxia telangiectasia patients is associated with translocation at 14q11. A model for other T cell neoplasia (Q68824808) (← links)
• Breakage of the T cell receptor alpha chain locus in non malignant clones from patients with ataxia telangiectasia (Q70059881) (← links)
• DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome (Q70072998) (← links)
• Human alpha-globin maps to pter-p13.3 in chromosome 16 distal to PGP (Q70182727) (← links)
• Somatic cell genetics and gene mapping (Q71168536) (← links)
• Comparative analysis of mouse-human hybrids with rearranged chromosomes 1 by in situ hybridization and southern blotting: High-resolution mapping of NRAS, NGFB, and AMY on human chromosome 1 (Q72751923) (← links)