Dewald GW - Search Results

1

A genetic review of complete and partial hydatidiform moles and nonmolar triploidy.

Lindor NM, Ney JA, Gaffey TA, Jenkins RB, Thibodeau SN, Dewald GW. Lindor NM, et al. Among authors: dewald gw. Mayo Clin Proc. 1992 Aug;67(8):791-9. doi: 10.1016/s0025-6196(12)60805-2. Mayo Clin Proc. 1992. PMID: 1434919 Review.

2

Mitomycin C chromosome stress test to identify hypersensitivity to bifunctional alkylating agents in patients with Fanconi anemia or aplastic anemia.

Kuffel DG, Lindor NM, Litzow MR, Zinsmeister AR, Dewald GW. Kuffel DG, et al. Among authors: dewald gw. Mayo Clin Proc. 1997 Jun;72(6):579-80. doi: 10.4065/72.6.579. Mayo Clin Proc. 1997. PMID: 9179145 No abstract available.

3

Fluorescent in situ hybridization: use of whole chromosome paint probes to identify unbalanced chromosome translocations.

Kraker WJ, Borell TJ, Schad CR, Pennington MJ, Karnes PS, Dewald GW, Jenkins RB. Kraker WJ, et al. Among authors: dewald gw. Mayo Clin Proc. 1992 Jul;67(7):658-62. doi: 10.1016/s0025-6196(12)60721-6. Mayo Clin Proc. 1992. PMID: 1434900

4

Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy.

Jalal SM, Lindor NM, Michels VV, Buckley DD, Hoppe DA, Sarkar G, Dewald GW. Jalal SM, et al. Among authors: dewald gw. Am J Med Genet. 1993 Jun 1;46(4):441-3. doi: 10.1002/ajmg.1320460419. Am J Med Genet. 1993. PMID: 8357018

5

Karyotypic analysis in primary myelodysplastic syndromes.

Noël P, Tefferi A, Pierre RV, Jenkins RB, Dewald GW. Noël P, et al. Among authors: dewald gw. Blood Rev. 1993 Mar;7(1):10-8. doi: 10.1016/0268-960x(93)90019-z. Blood Rev. 1993. PMID: 8467227 Review.

6

Uniparental disomy in congenital disorders: a prospective study.

Lindor NM, Karnes PS, Michels VV, Dewald GW, Goerss J, Jalal S, Jenkins RB, Vockley G, Thibodeau SN. Lindor NM, et al. Among authors: dewald gw. Am J Med Genet. 1995 Aug 28;58(2):143-6. doi: 10.1002/ajmg.1320580210. Am J Med Genet. 1995. PMID: 8533805

7

Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism.

Lindor NM, Devries EM, Michels VV, Schad CR, Jalal SM, Donovan KM, Smithson WA, Kvols LK, Thibodeau SN, Dewald GW. Lindor NM, et al. Among authors: dewald gw. Clin Genet. 1996 Mar;49(3):124-9. doi: 10.1111/j.1399-0004.1996.tb03270.x. Clin Genet. 1996. PMID: 8737976

8

Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects.

Lindor NM, Michels VV, Hoppe DA, Driscoll DJ, Leavitt JA, Dewald GW. Lindor NM, et al. Among authors: dewald gw. Am J Med Genet. 1992 Sep 1;44(1):61-5. doi: 10.1002/ajmg.1320440115. Am J Med Genet. 1992. PMID: 1519653

9

Acute leukemia with abnormal thrombopoiesis and inversions of chromosome 3.

Jenkins RB, Tefferi A, Solberg LA Jr, Dewald GW. Jenkins RB, et al. Among authors: dewald gw. Cancer Genet Cytogenet. 1989 Jun;39(2):167-79. doi: 10.1016/0165-4608(89)90182-9. Cancer Genet Cytogenet. 1989. PMID: 2752370

10

A cytogenetic study of 53 human gliomas.

Jenkins RB, Kimmel DW, Moertel CA, Schultz CG, Scheithauer BW, Kelly PJ, Dewald GW. Jenkins RB, et al. Among authors: dewald gw. Cancer Genet Cytogenet. 1989 Jun;39(2):253-79. doi: 10.1016/0165-4608(89)90192-1. Cancer Genet Cytogenet. 1989. PMID: 2752377

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

264 results

Search Page