Mohandas TK - Search Results

1

Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).

Park JP, Moeschler JB, Hani VH, Hawk AB, Belloni DR, Noll WW, Mohandas TK. Park JP, et al. Among authors: mohandas tk. Am J Med Genet. 1998 Jun 30;78(2):134-9. Am J Med Genet. 1998. PMID: 9674903

2

Smith-Magenis syndrome resulting from a de novo direct insertion of proximal 17q into 17p11.2.

Park JP, Moeschler JB, Davies WS, Patel PI, Mohandas TK. Park JP, et al. Among authors: mohandas tk. Am J Med Genet. 1998 Apr 28;77(1):23-7. Am J Med Genet. 1998. PMID: 9557889

3

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.

Mohandas TK, Park JP, Spellman RA, Filiano JJ, Mamourian AC, Hawk AB, Belloni DR, Noll WW, Moeschler JB. Mohandas TK, et al. Am J Med Genet. 1999 Feb 12;82(4):294-300. Am J Med Genet. 1999. PMID: 10051161

4

Amplification of the MLL region in acute myeloid leukemia.

Park JP, Ladd SL, Ely P, Weiner NJ, Wojiski SA, Hawk AB, Noll WW, Mohandas TK. Park JP, et al. Among authors: mohandas tk. Cancer Genet Cytogenet. 2000 Sep;121(2):198-205. doi: 10.1016/s0165-4608(00)00256-9. Cancer Genet Cytogenet. 2000. PMID: 11063808

5

Diffuse large cell, B-cell type lymphoma with a novel translocation (2;22)(p23;q11.2).

Park JP, Curran MJ, Levy NB, Davis TH, Elliott JH, Mohandas TK. Park JP, et al. Among authors: mohandas tk. Cancer Genet Cytogenet. 1997 Jul 15;96(2):118-22. doi: 10.1016/s0165-4608(96)00281-6. Cancer Genet Cytogenet. 1997. PMID: 9216718

6

Molecular studies of an ependymoma-associated constitutional t(1;22)(p22;q11.2).

Rhodes CH, Call KM, Budarf ML, Barnoski BL, Bell CJ, Emanuel BS, Bigner SH, Park JP, Mohandas TK. Rhodes CH, et al. Among authors: mohandas tk. Cytogenet Cell Genet. 1997;78(3-4):247-52. doi: 10.1159/000134667. Cytogenet Cell Genet. 1997. PMID: 9465898

7

Human chromosome 9 pericentric homologies: implications for chromosome 9 heteromorphisms.

Park JP, Wojiski SA, Spellman RA, Rhodes CH, Mohandas TK. Park JP, et al. Among authors: mohandas tk. Cytogenet Cell Genet. 1998;82(3-4):192-4. doi: 10.1159/000015097. Cytogenet Cell Genet. 1998. PMID: 9858814

8

Estimate of prevalence of proximal 15q duplication syndrome.

Moeschler JB, Mohandas TK, Hawk AB, Noll WW. Moeschler JB, et al. Among authors: mohandas tk. Am J Med Genet. 2002 Sep 1;111(4):440-2. doi: 10.1002/ajmg.10419. Am J Med Genet. 2002. PMID: 12210307 No abstract available.

9

Assignment of acetyl-CoA carboxylase-beta (ACACB) to human chromosome band 12q24.1 by in situ hybridization.

Ullrich CK, Widmer J, Park JP, Mohandas TK, Witters LA. Ullrich CK, et al. Among authors: mohandas tk. Cytogenet Cell Genet. 1997;77(3-4):176-7. doi: 10.1159/000134568. Cytogenet Cell Genet. 1997. PMID: 9284908 No abstract available.

10

Assignment of the "spot 14" gene (THRSP) to human chromosome band 11q13.5 by in situ hybridization.

Moncur JT, Park JP, Maloney M, Mohandas TK, Kinlaw WB. Moncur JT, et al. Among authors: mohandas tk. Cytogenet Cell Genet. 1997;78(2):131-2. doi: 10.1159/000134644. Cytogenet Cell Genet. 1997. PMID: 9371405 No abstract available.

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