Borgaonkar D - Search Results

1

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.

Simon-Sanchez J, Scholz S, Fung HC, Matarin M, Hernandez D, Gibbs JR, Britton A, de Vrieze FW, Peckham E, Gwinn-Hardy K, Crawley A, Keen JC, Nash J, Borgaonkar D, Hardy J, Singleton A. Simon-Sanchez J, et al. Among authors: borgaonkar d. Hum Mol Genet. 2007 Jan 1;16(1):1-14. doi: 10.1093/hmg/ddl436. Epub 2006 Nov 20. Hum Mol Genet. 2007. PMID: 17116639

2

Y to X chromosome translocations.

Borgaonkar DS. Borgaonkar DS. Hum Genet. 1977 Dec 29;40(1):113-4. doi: 10.1007/BF00280838. Hum Genet. 1977. PMID: 564327 No abstract available.

3

Analysis of human chromosomal variants by quantitative electron microscopy. I. Group D chromosome with giant satellites.

Golomb HM, Bahr GF, Borgaonkar DS. Golomb HM, et al. Among authors: borgaonkar ds. Genetics. 1971 Sep;69(1):123-8. doi: 10.1093/genetics/69.1.123. Genetics. 1971. PMID: 5133082 Free PMC article. No abstract available.

4

Sister chromatid exchanges in balanced translocation carriers and in patients with unbalanced karyotypes.

Stoll C, Borgaonkar DS, Bigel P. Stoll C, et al. Among authors: borgaonkar ds. Hum Genet. 1977 Jun 10;37(1):27-32. doi: 10.1007/BF00293768. Hum Genet. 1977. PMID: 881193

5

Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).

Fu W, Borgaonkar DS, Ladewig PP, Weaver J, Pomerance HH. Fu W, et al. Among authors: borgaonkar ds. Clin Genet. 1976 Dec;10(6):329-36. doi: 10.1111/j.1399-0004.1976.tb00057.x. Clin Genet. 1976. PMID: 991443

6

Cytogenetic and linkage studies of a familial 15pplus variant.

Yoder FE, Bias WB, Borgaonkar DS, Bahr GF, Yoder II, Yoder OC, Golomb HM. Yoder FE, et al. Among authors: borgaonkar ds. Am J Hum Genet. 1974 Sep;26(5):535-48. Am J Hum Genet. 1974. PMID: 4138462 Free PMC article. No abstract available.

7

Analysis of human chromosomal variants by quantitative electron microscopy. II. Ring chromosome 18.

Golomb HM, Bahr GF, Borgaonkar DS. Golomb HM, et al. Among authors: borgaonkar ds. Chromosoma. 1971;34(1):94-8. doi: 10.1007/BF00285519. Chromosoma. 1971. PMID: 5568668 No abstract available.

8

Identification of a C6-G21 translocation chromosome by the Q-M and Giemsa banding techniques in a patient with Down's syndrome, with possible assignment of Gm locus.

Borgaonkar DS, Bias WB, Chase GA, Sadasivan G, Herr HM, Golomb HM, Bahr GF, Kunkel LM. Borgaonkar DS, et al. Clin Genet. 1973;4(1):53-7. doi: 10.1111/j.1399-0004.1973.tb01122.x. Clin Genet. 1973. PMID: 4120631 No abstract available.

9

Identification of a D-E(15-18) translocation chromosome by quinacrine fluorescence and urea banding techniques.

Borgaonkar DS, Ebenezer L, Scott CI Jr, Golomb HM, Bahr GF. Borgaonkar DS, et al. Humangenetik. 1973;17(4):317-21. doi: 10.1007/BF00273186. Humangenetik. 1973. PMID: 4694513 No abstract available.

10

Chromosomal variation in man: catalog of chromosomal variants and anomalies.

Borgaonkar DS, Bolling DR, Partridge C, Ruddle FH, McKusick VA. Borgaonkar DS, et al. Cytogenet Cell Genet. 1975;14(3-6):252-4. doi: 10.1159/000130355. Cytogenet Cell Genet. 1975. PMID: 1192796 No abstract available.

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