| 1 | GK, AHC, GKD, DELXP21
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| Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21.
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| Worley KC, et al.
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| Genomics 16 : 407-416. 1993
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| 2 | DELXP21, GK, GKD
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| Mental retardation locus in Xp21 chromosome microdeletion.
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| Fries MH, Lebo RV, Schonberg SA, Golabi M, Seltzer WK, Gitelman SE, Golbus MS.
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| Am J Med Genet 46(4):363-8. 1993
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| 3 | DELXP21, GKD
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| Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpoints.
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| McCabe ER, Towbin JA, van den Engh G, Trask BJ.
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| Am J Hum Genet 51(6):1277-85. 1992
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| 4 | AHC, DELXP21, GK, GKD
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| Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.
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| Francke U, Harper JF, Darras BT, Cowan JM, McCabe ER, Kohlsch�tter A, Seltzer WK, Saito F, Goto J, Harpey JP, et al.
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| Am J Hum Genet 40(3):212-27. 1987
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| 5 | DELXP21, GKD
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| Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies.
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| Clarke A, Roberts SH, Thomas NS, Whitfield A, Williams J, Harper PS.
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| J Med Genet 23(6):501-8. 1986
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