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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 1 |
1996 | 1 |
2005 | 1 |
2010 | 1 |
2011 | 2 |
2024 | 0 |
PubMed for id: 321949
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Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
Cytogenet Genome Res. 2011;132(4):233-8. doi: 10.1159/000321647. Epub 2010 Nov 10.
Cytogenet Genome Res. 2011.
PMID: 21063078
The Hunter-McAlpine syndrome results from duplication 5q35-qter.
Hunter AG, Dupont B, McLaughlin M, Hinton L, Baker E, Adès L, Haan E, Schwartz CE.
Hunter AG, et al.
Clin Genet. 2005 Jan;67(1):53-60. doi: 10.1111/j.1399-0004.2005.00378.x.
Clin Genet. 2005.
PMID: 15617549
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Hunter-McAlpine syndrome: report of a third family.
Adès LC, Morris LL, Simpson DA, Haan EA.
Adès LC, et al.
Clin Dysmorphol. 1993 Apr;2(2):123-30.
Clin Dysmorphol. 1993.
PMID: 8281273
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Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.
Thomas JA, Manchester DK, Prescott KE, Milner R, McGavran L, Cohen MM Jr.
Thomas JA, et al.
Am J Med Genet. 1996 Apr 24;62(4):372-5. doi: 10.1002/(SICI)1096-8628(19960424)62:4<372::AID-AJMG9>3.0.CO;2-T.
Am J Med Genet. 1996.
PMID: 8723067
Review.
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Ventricular noncompaction and absent thumbs in a newborn with tetrasomy 5q35.2-5q35.3: an association with Hunter-McAlpine syndrome?
Sellars EA, Zimmerman SL, Smolarek T, Hopkin RJ.
Sellars EA, et al.
Am J Med Genet A. 2011 Jun;155A(6):1409-13. doi: 10.1002/ajmg.a.33997. Epub 2011 May 12.
Am J Med Genet A. 2011.
PMID: 21567924
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