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3. Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations. Delezoide AL; Vekemans M Biomed Pharmacother; 1994; 48(8-9):335-9. PubMed ID: 7858167 [TBL] [Abstract][Full Text] [Related]
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8. Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects. Newton R; Stanier P; Loughna S; Henderson DJ; Forbes SA; Farrall M; Jensson O; Moore GE Clin Genet; 1994 May; 45(5):241-9. PubMed ID: 8076409 [TBL] [Abstract][Full Text] [Related]
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11. Finding genes involved in human developmental disorders. Muenke M Curr Opin Genet Dev; 1995 Jun; 5(3):354-61. PubMed ID: 7549431 [TBL] [Abstract][Full Text] [Related]
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15. Comparative gene mapping: a valuable new tool for mammalian developmental studies. Womack JE Dev Genet; 1987; 8(4):281-93. PubMed ID: 3502975 [TBL] [Abstract][Full Text] [Related]
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