相似文献
1
Hypoxanthine-guanine phosphoribosyltransferase deficiency and Xg blood group.
Am J Hum Genet. 1970 Jan;22(1):50-4.
2
Hypoxanthine-guanine phosphoribosyltransferase and deutan colour blindness: the relative positions of their loci on the X-chromosome.
Adv Exp Med Biol. 1973;41:281-3. doi: 10.1007/978-1-4684-3294-7_33.
3
Inheritance of hypoxanthine-guanine phosphoribosyltransferase deficiency and detection of heterozygotes.
Fed Proc. 1968 Jul-Aug;27(4):1085-6.
4
X-linked primary hyperuricaemia (hypoxanthine-guanine phosphoribosyltransferase deficiency encephalopathy.
J Ment Defic Res. 1968 Jun;12(2):100-7. doi: 10.1111/j.1365-2788.1968.tb00248.x.
5
6
Hypoxanthine-guanine phosphoribosyltransferase deficiency in the Lesch-Nyhan syndrome and gout.
Fed Proc. 1968 Jul-Aug;27(4):1047-52.
7
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase: intermediate enzyme deficiency in heterozygote red cells.
Ann Intern Med. 1972 Feb;76(2):285-7. doi: 10.7326/0003-4819-76-2-285.
8
Disorder of purine metabolism due to partial deficiency of hypoxanthine-guanine phosphoribosyltransferase. A study of a family.
Am J Med. 1970 Feb;48(2):148-61. doi: 10.1016/0002-9343(70)90111-7.
9
Phosphoribosyltransferase (PRT) and adenine PRT (A-PRT) deficiency states in man--new inborn errors of purine metabolism.
Ann Intern Med. 1969 Jan;70(1):229-30. doi: 10.7326/0003-4819-70-1-229.
10
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase associated with gout and uric acid lithiasis.
Rev Eur Etud Clin Biol. 1970 Nov;15(9):942-7.
引用本文的文献
1
The application of DNA recombinant technology to the analysis of the human genome and genetic disease.
Hum Genet. 1981;58(4):351-7. doi: 10.1007/BF00282814.
2
X-chromosome inactivation and the Xg locus.
Am J Hum Genet. 1970 Jul;22(4):460-3.
3
Absence of measurable linkage between the loci for hypoxanthine-guanine phosphoribosyltransferase and deutan colorblindness.
Am J Hum Genet. 1974 Jan;26(1):78-82.
4
Hypoxanthine-guanine phosphoribosyl transferase deficiency.
Hum Genet. 1976 Feb 29;31(2):127-50. doi: 10.1007/BF00296142.
本文引用的文献
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HEREDITARY CHOREOATHETOSIS, SELF-MUTILATION AND HYPERURICEMIA IN YOUNG MALES.
N Engl J Med. 1965 Jul 15;273:130-5. doi: 10.1056/NEJM196507152730303.
2
X CHROMOSOME MAPPING OF GENES FOR RED-GREEN COLORBLINDNESS AND XG.
Am J Hum Genet. 1964 Dec;16(4):403-9.
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A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION.
Am J Med. 1964 Apr;36:561-70. doi: 10.1016/0002-9343(64)90104-4.
4
THE LINKAGE RELATIONS OF HEMOPHILIA A AND HEMOPHILIA B (CHRISTMAS DISEASE) TO THE XG BLOOD GROUP SYSTEM.
Am J Hum Genet. 1963 Dec;15(4):481-92.
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Inherited disorder of purine metabolism. Correlation between central nervous system dysfunction and biochemical defects.
JAMA. 1967 Oct 16;202(3):175-7. doi: 10.1001/jama.202.3.175.
6
Deletion of the long arm of chromosome 16 and an unexpected Duffy blood group phenotype reveal a possible autosomal linkage.
Nature. 1967 Sep 2;215(5105):1075-6. doi: 10.1038/2151075a0.
7
A common X-linked serum marker and its relation to other loci on the X chromosome.
Trans Assoc Am Physicians. 1966;79:165-76.
8
The Xg blood groups and congenital hypogammaglobulinemia.
Vox Sang. 1965 Nov-Dec;10(6):729-30. doi: 10.1111/j.1423-0410.1965.tb05185.x.
9
A new disorder of purine metabolism with behavioral manifestations.
J Pediatr. 1969 Jan;74(1):20-7. doi: 10.1016/s0022-3476(69)80004-1.
10
Inheritance of purine phosphoribosyltransferases in man.
Am J Hum Genet. 1969 Jan;21(1):61-70.
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