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Robin C Schwartz MS, CGC

TitleAssistant Professor
InstitutionUConn Health Center
DepartmentGenetics and Developmental Biology
AddressMC 7120
UConn Health Partners, MC 7120
65 Kane Street
Phone860-523-6462
Fax860-523-6465
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    Other Positions
    TitleAssistant Professor
    InstitutionUConn Health Center
    DepartmentPediatrics


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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Felice KJ, Schwartz RC, Brown CA, Leicher CR, Grunnet ML. Autosomal dominant Emery-Dreifuss dystrophy due to mutations in rod domain of the lamin A/C gene. Neurology. 2000 Jul 25; 55(2):275-80. PMID: 10908904.
      View in: PubMed
    2. Schwartz RC, Blanton SH, Hyde CA, Sottile TR, Hudgins L, Sarfarazi M, Tsipouras P. Linkage analysis in Marfan syndrome. J Med Genet. 1990 Feb; 27(2):86-90. PMID: 1969490; PMCID: PMC1016926.
    3. Tsipouras P, Schwartz RC, Liddell AC, Salkeld CS, Weil D, Ramirez F. Genetic distance of two fibrillar collagen loci, COL3A1 and COL5A2, located on the long arm of human chromosome 2. Genomics. 1988 Oct; 3(3):275-7. PMID: 3224983.
      View in: PubMed
    4. Schwartz RC, Young MF, Tsipouras P. Two RFLPs in the 5' end of the human osteonectin (ON) gene. Nucleic Acids Res. 1988 Sep 26; 16(18):9076. PMID: 2902577; PMCID: PMC338686.
    5. Schwartz RC, Liddell A, Ramirez F, Tsipouras P. An RFLP in the gene for the human pro-alpha 2 chain of type V collagen (COL5A2). Nucleic Acids Res. 1988 Jun 10; 16(11):5225. PMID: 2898765; PMCID: PMC336759.
    6. Tsipouras P, Schwartz RC, Phillips JA, Willard HF. A centromere-based linkage group on the long arm of human chromosome 17. Cytogenet Cell Genet. 1988; 47(1-2):109-10. PMID: 3162714.
      View in: PubMed
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