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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1976 | 1 |
1990 | 2 |
1993 | 2 |
1999 | 2 |
2024 | 0 |
PubMed (OMIM) for id: 338045
7 results
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Southwestern Athabaskan (Navajo and Apache) genetic diseases.
Genet Med. 1999 May-Jun;1(4):151-7. doi: 10.1097/00125817-199905000-00007.
Genet Med. 1999.
PMID: 11258351
Free article.
Liver disease in Navajo neuropathy.
Holve S, Hu D, Shub M, Tyson RW, Sokol RJ.
Holve S, et al.
J Pediatr. 1999 Oct;135(4):482-93. doi: 10.1016/s0022-3476(99)70172-1.
J Pediatr. 1999.
PMID: 10518083
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The human homolog of the glomerulosclerosis gene Mpv17: structure and genomic organization.
Karasawa M, Zwacka RM, Reuter A, Fink T, Hsieh CL, Lichter P, Francke U, Weiher H.
Karasawa M, et al.
Hum Mol Genet. 1993 Nov;2(11):1829-34. doi: 10.1093/hmg/2.11.1829.
Hum Mol Genet. 1993.
PMID: 8281143
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Familial sensory autonomic neuropathy with arthropathy in Navajo children.
Johnsen SD, Johnson PC, Stein SR.
Johnsen SD, et al.
Neurology. 1993 Jun;43(6):1120-5. doi: 10.1212/wnl.43.6.1120.
Neurology. 1993.
PMID: 8170555
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Neuropathy in Navajo children: clinical and epidemiologic features.
Singleton R, Helgerson SD, Snyder RD, O'Conner PJ, Nelson S, Johnsen SD, Allanson JE.
Singleton R, et al.
Neurology. 1990 Feb;40(2):363-7. doi: 10.1212/wnl.40.2.363.
Neurology. 1990.
PMID: 2300261
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Transgenic mouse model of kidney disease: insertional inactivation of ubiquitously expressed gene leads to nephrotic syndrome.
Weiher H, Noda T, Gray DA, Sharpe AH, Jaenisch R.
Weiher H, et al.
Cell. 1990 Aug 10;62(3):425-34. doi: 10.1016/0092-8674(90)90008-3.
Cell. 1990.
PMID: 1696177
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Acromutilating, paralyzing neuropathy with corneal ulceration in Navajo children.
Appenzeller O, Kornfeld M, Snyder R.
Appenzeller O, et al.
Arch Neurol. 1976 Nov;33(11):733-8. doi: 10.1001/archneur.1976.00500110001001.
Arch Neurol. 1976.
PMID: 185990
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