Punnett HH - Search Results

1

A second case of myelodysplastic syndrome with t(9;12)(q22;p12).

Mahmoodi M, Swami VK, Besa EC, Punnett HH. Mahmoodi M, et al. Among authors: punnett hh. Cancer Genet Cytogenet. 2005 Mar;157(2):187-8. doi: 10.1016/j.cancergencyto.2004.08.002. Cancer Genet Cytogenet. 2005. PMID: 15721645 No abstract available.

2

Translocation (16;18)(p13;q21.3) in follicular lymphoma.

Mahmoodi M, Tanev SS, Punnett HH, Crilley P, Hou JS. Mahmoodi M, et al. Among authors: punnett hh. Cancer Genet Cytogenet. 2004 Oct 15;154(2):160-2. doi: 10.1016/j.cancergencyto.2004.02.008. Cancer Genet Cytogenet. 2004. PMID: 15474153

3

Clonal abnormalities in a recurrent laryngeal papilloma.

Soliman A, Khurana JS, Punnett HH. Soliman A, et al. Among authors: punnett hh. Cancer Genet Cytogenet. 2005 Jun;159(2):190-1. doi: 10.1016/j.cancergencyto.2004.11.001. Cancer Genet Cytogenet. 2005. PMID: 15899398 No abstract available.

4

Translocation 10;17 in clear cell sarcoma of the kidney. A first report.

Punnett HH, Halligan GE, Zaeri N, Karmazin N. Punnett HH, et al. Cancer Genet Cytogenet. 1989 Aug;41(1):123-8. doi: 10.1016/0165-4608(89)90116-7. Cancer Genet Cytogenet. 1989. PMID: 2548705

5

A (7;18) translocation. 46,XY. Repository identification No. GM-657.

Punnett HH, Kistenmacher ML, Miller RC, Greene AE, Coriell LL. Punnett HH, et al. Cytogenet Cell Genet. 1979;24(2):126. doi: 10.1159/000131366. Cytogenet Cell Genet. 1979. PMID: 477406 No abstract available.

6

An (X;1) translocation, balanced, 46 chromosomes. Repository identification no. GM-97.

Punnett HH, Kistermacher ML, Greene AE, Coriell LL. Punnett HH, et al. Cytogenet Cell Genet. 1974;13(4):406-7. doi: 10.1159/000130291. Cytogenet Cell Genet. 1974. PMID: 4139001 No abstract available.

7

Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia.

Morrissette JJ, Halligan GE, Punnett HH, McKenzie AS, Guerrero F, de Chadarévian JP. Morrissette JJ, et al. Among authors: punnett hh. Cancer Genet Cytogenet. 2006 Aug;169(1):58-61. doi: 10.1016/j.cancergencyto.2006.02.007. Cancer Genet Cytogenet. 2006. PMID: 16875938

8

Simpson-Golabi-Behmel syndrome (SGBS) in a female with an X-autosome translocation.

Punnett HH. Punnett HH. Am J Med Genet. 1994 May 1;50(4):391-3. doi: 10.1002/ajmg.1320500424. Am J Med Genet. 1994. PMID: 8209925 No abstract available.

9

FOXO1-FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma.

Liu J, Guzman MA, Pezanowski D, Patel D, Hauptman J, Keisling M, Hou SJ, Papenhausen PR, Pascasio JM, Punnett HH, Halligan GE, de Chadarévian JP. Liu J, et al. Among authors: punnett hh. Mod Pathol. 2011 Oct;24(10):1327-35. doi: 10.1038/modpathol.2011.98. Epub 2011 Jun 10. Mod Pathol. 2011. PMID: 21666686 Free article.

10

Co-occurrence of non-mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: case report and review of the literature.

Kehinde FI, Anderson CE, McGowan JE, Jethva RN, Wahab MA, Glick AR, Sterner MR Jr, Pascasio JM, Punnett HH, Liu J. Kehinde FI, et al. Among authors: punnett hh. Am J Med Genet A. 2014 Dec;164A(12):3187-93. doi: 10.1002/ajmg.a.36778. Epub 2014 Sep 24. Am J Med Genet A. 2014. PMID: 25257307 Review.

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