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4. Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues. Pasteris NG; Gorski JL Genomics; 1999 Aug; 60(1):57-66. PubMed ID: 10458911 [TBL] [Abstract][Full Text] [Related]
5. Cloning and mapping of the XRN2 gene to human chromosome 20p11.1-p11.2. Zhang M; Yu L; Xin Y; Hu P; Fu Q; Yu C; Zhao S Genomics; 1999 Jul; 59(2):252-4. PubMed ID: 10409438 [TBL] [Abstract][Full Text] [Related]
6. Cloning of a novel member of the reticulon gene family (RTN3): gene structure and chromosomal localization to 11q13. Moreira EF; Jaworski CJ; Rodriguez IR Genomics; 1999 May; 58(1):73-81. PubMed ID: 10331947 [TBL] [Abstract][Full Text] [Related]
7. Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes. Pappano WN; Scott IC; Clark TG; Eddy RL; Shows TB; Greenspan DS Genomics; 1998 Sep; 52(2):236-9. PubMed ID: 9782094 [TBL] [Abstract][Full Text] [Related]
8. Cloning and characterization of a novel human gene, TM4SF6, encoding a protein belonging to the transmembrane 4 superfamily, and mapped to Xq22. Maeda K; Matsuhashi S; Hori K; Xin Z; Mukai T; Tabuchi K; Egashira M; Niikawa N Genomics; 1998 Sep; 52(2):240-2. PubMed ID: 9782095 [No Abstract] [Full Text] [Related]
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14. Rat neurological mutations cerebellar vermis defect and hobble are caused by mutations in the netrin-1 receptor gene Unc5h3. Kuramoto T; Kuwamura M; Serikawa T Brain Res Mol Brain Res; 2004 Mar; 122(2):103-8. PubMed ID: 15010202 [TBL] [Abstract][Full Text] [Related]
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