Ing PS - Search Results

1

Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices.

Caudill SP, Van Dyke DL, Chen AT, Reidy JA, Ing PS, Schwartz S, Vance GH. Caudill SP, et al. Among authors: ing ps. Stat Med. 2005 Feb 28;24(4):615-22. doi: 10.1002/sim.2040. Stat Med. 2005. PMID: 15678412

2

Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.

Ing PS, Van Dyke DL, Caudill SP, Reidy JA, Bice G, Bieber FR, Buchanan PD, Carroll AJ, Cheung SW, DeWald G, Donahue RP, Gardner HA, Higgins J, Hsu LY, Jamehdor M, Keitges EA, Laundon CH, Luthardt FW, Mascarello J, May KM, Meck JM, Morton C, Patil S, Peakman D, Pettenati MJ, Rao N, Sanger WG, Saxe DF, Schwartz S, Sekhon GS, Vance GH, Wyandt HE, Yu CW, Zenger-Hain J, Chen AT. Ing PS, et al. Genet Med. 1999 Mar-Apr;1(3):94-7. doi: 10.1097/00125817-199903000-00006. Genet Med. 1999. PMID: 11336459 Free article.

3

The ACMG CYTO2000 subcommittee?

Chen AT, Ing PS, Reidy JA, Schwartz S, Vance GH, Van Dyke DL. Chen AT, et al. Among authors: ing ps. Genet Med. 1998 Nov-Dec;1(1):67. doi: 10.1097/00125817-199811000-00026. Genet Med. 1998. PMID: 11261434 Free article. No abstract available.

4

Cat-eye syndrome with different marker chromosomes in a mother and daughter.

Ing PS, Lubinsky MS, Smith SD, Golden E, Sanger WG, Duncan AM. Ing PS, et al. Am J Med Genet. 1987 Mar;26(3):621-8. doi: 10.1002/ajmg.1320260317. Am J Med Genet. 1987. PMID: 3105314

5

Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.

Kimberling WJ, Weston MD, Möller C, van Aarem A, Cremers CW, Sumegi J, Ing PS, Connolly C, Martini A, Milani M, et al. Kimberling WJ, et al. Among authors: ing ps. Am J Hum Genet. 1995 Jan;56(1):216-23. Am J Hum Genet. 1995. PMID: 7825581 Free PMC article.

6

Cytogenetic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y;13) translocation showing differential centromeric activity.

Ing PS, Smith SD. Ing PS, et al. Clin Genet. 1983 Sep;24(3):194-9. doi: 10.1111/j.1399-0004.1983.tb02239.x. Clin Genet. 1983. PMID: 6627723

7

Availability of genetic services to the deaf.

Ing PS, Lempke ML, Smith SD, Kimberling WJ. Ing PS, et al. Am J Med Genet. 1989 Oct;34(2):300-1. doi: 10.1002/ajmg.1320340239. Am J Med Genet. 1989. PMID: 2530902 No abstract available.

8

A comment on the analysis of families with prelinqual deafness.

Kimberling S, Smith SD, Ing PS, Tinley S. Kimberling S, et al. Among authors: ing ps. Am J Hum Genet. 1989 Jul;45(1):157-60. Am J Hum Genet. 1989. PMID: 2741946 Free PMC article. No abstract available.

9

Familial dyslexia: use of genetic linkage data to define subtypes.

Smith SD, Pennington BF, Kimberling WJ, Ing PS. Smith SD, et al. Among authors: ing ps. J Am Acad Child Adolesc Psychiatry. 1990 Mar;29(2):204-13. doi: 10.1097/00004583-199003000-00008. J Am Acad Child Adolesc Psychiatry. 1990. PMID: 1969860

10

National Deaf Register as a resource for hereditary deafness research.

Ing PS, Wernimont BM, Smith SD, Kimberling WJ. Ing PS, et al. Ann N Y Acad Sci. 1991;630:292. doi: 10.1111/j.1749-6632.1991.tb19609.x. Ann N Y Acad Sci. 1991. PMID: 1952610 No abstract available.

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