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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1998 | 1 |
2000 | 1 |
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2003 | 1 |
2007 | 1 |
2015 | 1 |
2024 | 0 |
PubMed for id: 871190
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Page 1
De novo 11q13.4q14.3 tetrasomy with uniparental isodisomy for 11q14.3qter.
Am J Med Genet A. 2015 Oct;167A(10):2327-33. doi: 10.1002/ajmg.a.37179. Epub 2015 Jun 10.
Am J Med Genet A. 2015.
PMID: 26061664
Cerebellar atrophy in Schimke-immuno-osseous dysplasia.
Lücke T, Clewing JM, Boerkoel CF, Hartmann H, Das AM, Knauth M, Becker H, Donnerstag F.
Lücke T, et al.
Am J Med Genet A. 2007 Sep 1;143A(17):2040-5. doi: 10.1002/ajmg.a.31878.
Am J Med Genet A. 2007.
PMID: 17676601
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Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.
Triki C, Louhichi N, Méziou M, Choyakh F, Kéchaou MS, Jlidi R, Mhiri C, Fakhfakh F, Ayadi H.
Triki C, et al.
Neuromuscul Disord. 2003 Jan;13(1):4-12. doi: 10.1016/s0960-8966(02)00188-8.
Neuromuscul Disord. 2003.
PMID: 12467726
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Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.
Chen CP, Chang TY, Shih JC, Lin SP, Lin CJ, Wang W, Lee CC, Town DD, Pan CW, Tzen CY.
Chen CP, et al.
Prenat Diagn. 2002 Dec;22(12):1063-6. doi: 10.1002/pd.459.
Prenat Diagn. 2002.
PMID: 12454959
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Absence of 9q22-9qter in trisomy 9 does not prevent a Dandy-Walker phenotype.
von Kaisenberg CS, Caliebe A, Krams M, Hackelöer BJ, Jonat W.
von Kaisenberg CS, et al.
Am J Med Genet. 2000 Dec 18;95(5):425-8.
Am J Med Genet. 2000.
PMID: 11146460
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[Joubert syndrome: a report of 5 cases].
Calleja-Pérez B, Fernández-Jaén A, Martínez-Bermejo A, Pascual-Castroviejo I.
Calleja-Pérez B, et al.
Rev Neurol. 1998 Apr;26(152):548-50.
Rev Neurol. 1998.
PMID: 9796002
Spanish.
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