These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
25. Linkage analysis in three families with nonspecific X-linked mental retardation. Claes S; Gu XX; Legius E; Lorenzetti E; Marynen P; Fryns JP; Cassiman JJ; Raeymaekers P Am J Med Genet; 1996 Jul; 64(1):137-46. PubMed ID: 8826464 [TBL] [Abstract][Full Text] [Related]
26. X-linked dominant chondrodysplasia punctata: a case report and family studies. Mueller RF; Crowle PM; Jones RA; Davison BC Am J Med Genet; 1985 Jan; 20(1):137-44. PubMed ID: 4038582 [TBL] [Abstract][Full Text] [Related]
27. Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females. Renault NK; Dyack S; Dobson MJ; Costa T; Lam WL; Greer WL Eur J Hum Genet; 2007 Jun; 15(6):628-37. PubMed ID: 17342157 [TBL] [Abstract][Full Text] [Related]
28. X-linked laterality sequence in a family with carrier manifestations. Mikkilä SP; Janas M; Karikoski R; Tarkkila T; Simola KO Am J Med Genet; 1994 Feb; 49(4):435-8. PubMed ID: 8160739 [TBL] [Abstract][Full Text] [Related]
29. A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26. Priest JM; Fischbeck KH; Nouri N; Keats BJ Genomics; 1995 Sep; 29(2):409-12. PubMed ID: 8666389 [TBL] [Abstract][Full Text] [Related]
30. [A family with thyroxine-binding globulin deficiency]. Mitsuno M; Takada H; Imashuku S; Kusunoki T; Miyazaki T Horumon To Rinsho; 1975 Jun; 23(6):517-20. PubMed ID: 807444 [No Abstract] [Full Text] [Related]
31. Linkage of thyroxine-binding globulin deficiency to other X-chromosome loci. Bode HH; Rothman KJ; Danon M J Clin Endocrinol Metab; 1973 Jul; 37(1):25-9. PubMed ID: 4197606 [No Abstract] [Full Text] [Related]
34. Protein deficiency in three generations of one family. Zauber NP; Kudryk AB N J Med; 1988 Oct; 85(10):805-7. PubMed ID: 3226628 [No Abstract] [Full Text] [Related]
36. X-chromosome linked inheritance of thyroxine-binding globulin deficiency. Nikolai TF; Seal US J Clin Endocrinol Metab; 1967 Nov; 27(11):1515-20. PubMed ID: 4965464 [No Abstract] [Full Text] [Related]
37. X-chromosome linked inheritance of elevated thyroxine-binding globulin in association with goiter. Shane SR; Seal US; Jones JE J Clin Endocrinol Metab; 1971 May; 32(5):587-94. PubMed ID: 4996058 [No Abstract] [Full Text] [Related]