Silverman GA - Search Results

1

(CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein.

Khurana TS, Engle EC, Bennett RR, Silverman GA, Selig S, Bruns GA, Kunkel LM. Khurana TS, et al. Among authors: silverman ga. Hum Mol Genet. 1994 May;3(5):841. doi: 10.1093/hmg/3.5.841-a. Hum Mol Genet. 1994. PMID: 8081380 No abstract available.

2

The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.

Silverman GA, Schneider SS, Massa HF, Flint A, Lalande M, Leonard JC, Overhauser J, van den Engh G, Trask BJ. Silverman GA, et al. Am J Hum Genet. 1995 Apr;56(4):926-37. Am J Hum Genet. 1995. PMID: 7717403 Free PMC article.

3

Reassignment of pEFD70.3 (D18S23) to human chromosome band 21q22.2 (D21S412) by physical mapping.

Silverman GA, Jenkins R, Bruns GA, LeBeau MM. Silverman GA, et al. Hum Mol Genet. 1993 Mar;2(3):331. doi: 10.1093/hmg/2.3.331. Hum Mol Genet. 1993. PMID: 8499926 No abstract available.

4

pMCT108.2 is a chimaeric clone which physically maps to human chromosome bands 9q33 (D9S203) and 18q21.1 (D18S24).

Lia KM, Bruns GA, LeBeau MM, Silverman GA. Lia KM, et al. Among authors: silverman ga. Hum Mol Genet. 1993 Mar;2(3):332. doi: 10.1093/hmg/2.3.332. Hum Mol Genet. 1993. PMID: 8499927 No abstract available.

5

Report of the Fourth International Workshop on Human Chromosome 18 Mapping. Boston, Massachusetts, October 7-9, 1996.

Silverman GA, Overhauser J, Gerken S, Aburomia R, O'Connell P, Krauter KS, Detera-Wadleigh SD, Yoshikawa T, Collins AR, Geurts van Kessel A. Silverman GA, et al. Cytogenet Cell Genet. 1996;75(2-3):111-31. doi: 10.1159/000134462. Cytogenet Cell Genet. 1996. PMID: 9040777 No abstract available.

6

An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA.

Katz SG, Schneider SS, Bartuski A, Trask BJ, Massa H, Overhauser J, Lalande M, Lansdorp PM, Silverman GA. Katz SG, et al. Among authors: silverman ga. Hum Mol Genet. 1999 Jan;8(1):87-92. doi: 10.1093/hmg/8.1.87. Hum Mol Genet. 1999. PMID: 9887335

7

Macrocephaly and developmental delay caused by missense variants in RAB5C.

Koop K, Yuan W, Tessadori F, Rodriguez-Polanco WR, Grubbs J, Zhang B, Osmond M, Graham G, Sawyer S, Conboy E, Vetrini F, Treat K, Płoski R, Pienkowski VM, Kłosowska A, Fieg E, Krier J, Mallebranche C, Alban Z, Aldinger KA, Ritter D, Macnamara E, Sullivan B, Herriges J, Alaimo JT, Helbig C, Ellis CA, van Eyk C, Gecz J, Farrugia D, Osei-Owusu I, Adès L, van den Boogaard MJ, Fuchs S, Bakker J, Duran K, Dawson ZD, Lindsey A, Huang H, Baldridge D, Silverman GA, Grant BD, Raizen D; Undiagnosed Diseases Network; van Haaften G, Pak SC, Rehmann H, Schedl T, van Hasselt P. Koop K, et al. Among authors: silverman ga. Hum Mol Genet. 2023 Oct 17;32(21):3063-3077. doi: 10.1093/hmg/ddad130. Hum Mol Genet. 2023. PMID: 37552066 Free PMC article.

8

Integration of 28 STSs into the physical map of human chromosome 18.

Gerken S, Fish K, Uyar D, Polymeropoulos MH, Bradley P, White R, Overhauser J, Silverman GA. Gerken S, et al. Among authors: silverman ga. Genomics. 1994 Dec;24(3):612-3. doi: 10.1006/geno.1994.1679. Genomics. 1994. PMID: 7713522 No abstract available.

9

A serine proteinase inhibitor locus at 18q21.3 contains a tandem duplication of the human squamous cell carcinoma antigen gene.

Schneider SS, Schick C, Fish KE, Miller E, Pena JC, Treter SD, Hui SM, Silverman GA. Schneider SS, et al. Among authors: silverman ga. Proc Natl Acad Sci U S A. 1995 Apr 11;92(8):3147-51. doi: 10.1073/pnas.92.8.3147. Proc Natl Acad Sci U S A. 1995. PMID: 7724531 Free PMC article.

10

Isolating vector-insert junctions from yeast artificial chromosomes.

Silverman GA. Silverman GA. PCR Methods Appl. 1993 Dec;3(3):141-50. doi: 10.1101/gr.3.3.141. PCR Methods Appl. 1993. PMID: 8118395 Free article. Review. No abstract available.

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