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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
88 related items for PubMed ID: 2031615
21. Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23. Stuhrmann M, Hennies HC, Bukhari IA, Brakensiek K, Nürnberg G, Becker C, Huebener J, Miranda MC, Frye-Boukhriss H, Knothe S, Schmidtke J, El-Harith EH. Clin Genet; 2008 Jun; 73(6):566-72. PubMed ID: 18462451 [Abstract] [Full Text] [Related]
22. Primary spontaneous pneumothorax in two siblings suggests autosomal recessive inheritance. Koivisto PA, Mustonen A. Chest; 2001 May; 119(5):1610-2. PubMed ID: 11348979 [Abstract] [Full Text] [Related]
23. Gonadal mosaicism as a rare cause of autosomal recessive inheritance. Anazi S, Al-Sabban E, Alkuraya FS. Clin Genet; 2014 Mar; 85(3):278-81. PubMed ID: 23551117 [Abstract] [Full Text] [Related]
24. Nonsyndromal anencephaly: possible autosomal recessive variant. Farag TI, Teebi AS, Al-Awadi SA. Am J Med Genet; 1986 Jul; 24(3):461-4. PubMed ID: 3728564 [Abstract] [Full Text] [Related]
25. Consanguinity increases the risk for aggressive periodontitis. Çalışır M. J Periodontal Res; 2018 Oct; 53(5):902-909. PubMed ID: 29947052 [Abstract] [Full Text] [Related]
26. Shadow autozygosity mapping by linkage exclusion (SAMPLE): a simple strategy to identify the genetic basis of lethal autosomal recessive disorders. Carr IM, Szymanska K, Sheridan E, Markham AF, Bonthron DT, Johnson CA. Hum Mutat; 2009 Dec; 30(12):1642-9. PubMed ID: 19842213 [Abstract] [Full Text] [Related]
27. Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis. De Koning TJ, Sandkuijl LA, De Schryver JE, Hennekam EA, Beemer FA, Houwen RH. Am J Med Genet; 1995 Jul 03; 57(3):479-82. PubMed ID: 7677155 [Abstract] [Full Text] [Related]
29. Identification of autosomal recessive disease loci using out-bred nuclear families. Carr IM, Diggle CP, Touqan N, Anwar R, Sheridan EG, Bonthron DT, Johnson CA, Ali M, Markham AF. Hum Mutat; 2012 Feb 03; 33(2):338-42. PubMed ID: 22052625 [Abstract] [Full Text] [Related]
30. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia. Naeem M, Muhammad D, Ahmad W. Br J Dermatol; 2005 Jul 03; 153(1):46-50. PubMed ID: 16029325 [Abstract] [Full Text] [Related]
31. [Truncus arteriosus: an autosomal recessive disease?]. le Marec B, Odent S, Almange C, Journel H, Roussey M, Defawe G. J Genet Hum; 1989 Sep 03; 37(3):225-30. PubMed ID: 2625625 [Abstract] [Full Text] [Related]
33. Exocrine pancreatic insufficiency in the Eurasian dog breed--inheritance and exclusion of two candidate genes. Proschowsky HF, Fredholm M. Anim Genet; 2007 Apr 03; 38(2):171-3. PubMed ID: 17302791 [Abstract] [Full Text] [Related]
34. Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33. Gabreëls-Festen A, van Beersum S, Eshuis L, LeGuern E, Gabreëls F, van Engelen B, Mariman E. J Neurol Neurosurg Psychiatry; 1999 May 03; 66(5):569-74. PubMed ID: 10209165 [Abstract] [Full Text] [Related]