Chromosomes, Human, Pair 4
This graph shows the total number of publications written about "Chromosomes, Human, Pair 4" by people in the URMC Research Network by year, and whether "Chromosomes, Human, Pair 4" was a major or minor topic of these publication.
Below are the most recent publications written about "Chromosomes, Human, Pair 4" by people in Profiles.
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Axford MM, López-Castel A, Nakamori M, Thornton CA, Pearson CE. Replacement of the myotonic dystrophy type 1 CTG repeat with 'non-CTG repeat' insertions in specific tissues. J Med Genet. 2011 Jul; 48(7):438-43.
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Al-Owain M, Kaya N, Al-Zaidan H, Bin Hussain I, Al-Manea H, Al-Hindi H, Kennedy S, Iqbal MA, Al-Mojalli H, Al-Bakheet A, Puel A, Casanova JL, Al-Muhsen S. Renal failure associated with APECED and terminal 4q deletion: evidence of autoimmune nephropathy. Clin Dev Immunol. 2010; 2010:586342.
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Paulsen JS, Langbehn DR, Stout JC, Aylward E, Ross CA, Nance M, Guttman M, Johnson S, MacDonald M, Beglinger LJ, Duff K, Kayson E, Biglan K, Shoulson I, Oakes D, Hayden M. Detection of Huntington's disease decades before diagnosis: the Predict-HD study. J Neurol Neurosurg Psychiatry. 2008 Aug; 79(8):874-80.
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Deak KL, Lemmers RJ, Stajich JM, Klooster R, Tawil R, Frants RR, Speer MC, van der Maarel SM, Gilbert JR. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4. Neurology. 2007 Feb 20; 68(8):578-82.
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Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology. 2007 Feb 20; 68(8):569-77.
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Tawil R, Van Der Maarel SM. Facioscapulohumeral muscular dystrophy. Muscle Nerve. 2006 Jul; 34(1):1-15.
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Al-Qurashi FH, Owaidah T, Iqbal MA, Aljurf M. Trisomy 4 as the sole karyotypic abnormality in a case of acute biphenotypic leukemia with T-lineage markers in minimally differentiated acute myelocytic leukemia. Cancer Genet Cytogenet. 2004 Apr 1; 150(1):66-9.
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Tawil R. Facioscapulohumeral muscular dystrophy. Curr Neurol Neurosci Rep. 2004 Jan; 4(1):51-4.
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Orrell RW, Tawil R, Forrester J, Kissel JT, Mendell JR, Figlewicz DA. Definitive molecular diagnosis of facioscapulohumeral dystrophy. Neurology. 1999 Jun 10; 52(9):1822-6.
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Ott S, Borchert M, Chung M, Appukuttan B, Wang X, Weinberg K, Stout JT. Exclusion of candidate genetic loci for Duane retraction syndrome. Am J Ophthalmol. 1999 Mar; 127(3):358-60.
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