Zinn AB - Search Results

1

The clinical introduction of genetic testing for Alzheimer disease. An ethical perspective.

Post SG, Whitehouse PJ, Binstock RH, Bird TD, Eckert SK, Farrer LA, Fleck LM, Gaines AD, Juengst ET, Karlinsky H, Miles S, Murray TH, Quaid KA, Relkin NR, Roses AD, St George-Hyslop PH, Sachs GA, Steinbock B, Truschke EF, Zinn AB. Post SG, et al. Among authors: zinn ab. JAMA. 1997 Mar 12;277(10):832-6. doi: 10.1001/jama.277.10.832. JAMA. 1997. PMID: 9052715 Review.

2

The need for anonymous genetic counseling and testing.

Mehlman MJ, Kodish ED, Whitehouse P, Zinn AB, Sollitto S, Berger J, Chiao EJ, Dosick MS, Cassidy SB. Mehlman MJ, et al. Among authors: zinn ab. Am J Hum Genet. 1996 Feb;58(2):393-7. Am J Hum Genet. 1996. PMID: 8571966 Free PMC article.

3

Distal deletion of the short arm of chromosome 6.

Zurcher VL, Golden WL, Zinn AB. Zurcher VL, et al. Among authors: zinn ab. Am J Med Genet. 1990 Feb;35(2):261-5. doi: 10.1002/ajmg.1320350223. Am J Med Genet. 1990. PMID: 2309766

4

Maternal uniparental disomy chromosome 14: case report and literature review.

Falk MJ, Curtis CA, Bass NE, Zinn AB, Schwartz S. Falk MJ, et al. Among authors: zinn ab. Pediatr Neurol. 2005 Feb;32(2):116-20. doi: 10.1016/j.pediatrneurol.2004.07.007. Pediatr Neurol. 2005. PMID: 15664772 Review.

5

Sex chromosome markers: characterization using fluorescence in situ hybridization and review of the literature.

Schwartz S, Depinet TW, Leana-Cox J, Isada NB, Karson EM, Park VM, Pasztor LM, Sheppard LC, Stallard R, Wolff DJ, Zinn AB, Zurcher VL, Zackowski JL. Schwartz S, et al. Among authors: zinn ab. Am J Med Genet. 1997 Jul 11;71(1):1-7. doi: 10.1002/(sici)1096-8628(19970711)71:1<1::aid-ajmg1>3.0.co;2-1. Am J Med Genet. 1997. PMID: 9215760 Review.

6

A 13-year-old boy with cognitive impairment, retinoblastoma, and Wilson disease.

Riley D, Wiznitzer M, Schwartz S, Zinn AB. Riley D, et al. Among authors: zinn ab. Neurology. 2001 Jul 10;57(1):141-3. doi: 10.1212/wnl.57.1.141. Neurology. 2001. PMID: 11445646

7

Inherited WT1 mutation in Denys-Drash syndrome.

Coppes MJ, Liefers GJ, Higuchi M, Zinn AB, Balfe JW, Williams BR. Coppes MJ, et al. Among authors: zinn ab. Cancer Res. 1992 Nov 1;52(21):6125-8. Cancer Res. 1992. PMID: 1327525

8

Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.

Depinet TW, Zackowski JL, Earnshaw WC, Kaffe S, Sekhon GS, Stallard R, Sullivan BA, Vance GH, Van Dyke DL, Willard HF, Zinn AB, Schwartz S. Depinet TW, et al. Among authors: zinn ab. Hum Mol Genet. 1997 Aug;6(8):1195-204. doi: 10.1093/hmg/6.8.1195. Hum Mol Genet. 1997. PMID: 9259264

9

Recurrent immune cytopenias in two patients with DiGeorge/velocardiofacial syndrome.

DePiero AD, Lourie EM, Berman BW, Robin NH, Zinn AB, Hostoffer RW. DePiero AD, et al. Among authors: zinn ab. J Pediatr. 1997 Sep;131(3):484-6. doi: 10.1016/s0022-3476(97)80085-6. J Pediatr. 1997. PMID: 9329436

10

Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13.

Mehra S, Christ L, Jeng L, Zinn AB, Schwartz S. Mehra S, et al. Among authors: zinn ab. Am J Med Genet A. 2005 Aug 30;137(2):217-21. doi: 10.1002/ajmg.a.30866. Am J Med Genet A. 2005. PMID: 16059944 Review.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

29 results

Search Page

Filters