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Year | Number of Results |
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1981 | 1 |
1997 | 1 |
2001 | 1 |
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2009 | 2 |
2024 | 0 |
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Page 1
XY Sex-reversed campomelia.
Eur J Pediatr. 1981 Sep;137(1):59-61. doi: 10.1007/BF00441171.
Eur J Pediatr. 1981.
PMID: 7274302
No abstract available.
Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1.
Krepischi-Santos AC, Rajan D, Temple IK, Shrubb V, Crolla JA, Huang S, Beal S, Otto PA, Carter NP, Vianna-Morgante AM, Rosenberg C.
Krepischi-Santos AC, et al. Among authors: shrubb v.
Cytogenet Genome Res. 2009;125(1):1-7. doi: 10.1159/000218743. Epub 2009 Jul 14.
Cytogenet Genome Res. 2009.
PMID: 19617690
Free PMC article.
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Opinion statement on the minimal acceptable standards of healthcare in cerebral palsy.
Bakheit AM, Bower E, Cosgrove A, Fox M, Morton R, Phillips S, Scrutton D, Shrubb V, Yude C.
Bakheit AM, et al. Among authors: shrubb v.
Disabil Rehabil. 2001 Sep 10;23(13):578-82. doi: 10.1080/09638280010029912.
Disabil Rehabil. 2001.
PMID: 11451192
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Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14.
Temple IK, Shrubb V, Lever M, Bullman H, Mackay DJ.
Temple IK, et al. Among authors: shrubb v.
J Med Genet. 2007 Oct;44(10):637-40. doi: 10.1136/jmg.2007.050807. Epub 2007 Jun 29.
J Med Genet. 2007.
PMID: 17601927
Free PMC article.
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Chronic bullous disease of childhood--another cause for potential misdiagnosis of sexual abuse?
Coleman H, Shrubb VA.
Coleman H, et al. Among authors: shrubb va.
Br J Gen Pract. 1997 Aug;47(421):507-8.
Br J Gen Pract. 1997.
PMID: 9302793
Free PMC article.
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Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14.
Temple IK, Shrubb V, Lever M, Bullman H, Mackay DJ.
Temple IK, et al. Among authors: shrubb v.
BMJ Case Rep. 2009;2009:bcr06.2009.1997. doi: 10.1136/bcr.06.2009.1997. Epub 2009 Jul 1.
BMJ Case Rep. 2009.
PMID: 21731585
Free PMC article.
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