Mowery-Rushton P[au] - Search Results

Year	Number of Results
1994	1
1995	1
1996	4
1997	2
2000	2
2002	2
2005	1
2016	1
2018	1
2024	0

1

Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis.

Prasad A, Sdano MA, Vanzo RJ, Mowery-Rushton PA, Serrano MA, Hensel CH, Wassman ER. Prasad A, et al. Among authors: mowery rushton pa. BMC Med Genet. 2018 Mar 20;19(1):46. doi: 10.1186/s12881-018-0555-3. BMC Med Genet. 2018. PMID: 29554876 Free PMC article.

2

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Ho KS, Twede H, Vanzo R, Harward E, Hensel CH, Martin MM, Page S, Peiffer A, Mowery-Rushton P, Serrano M, Wassman ER. Ho KS, et al. Among authors: mowery rushton p. Biomed Res Int. 2016;2016:3284534. doi: 10.1155/2016/3284534. Epub 2016 Nov 16. Biomed Res Int. 2016. PMID: 27975050 Free PMC article.

3

Fetal-type hepatoblastoma and del(3)(q11.2q13.2).

Sandoval C, Piper J, Mowery-Rushton PA, Jayabose S. Sandoval C, et al. Among authors: mowery rushton pa. Cancer Genet Cytogenet. 2002 Apr 15;134(2):162-4. doi: 10.1016/s0165-4608(01)00622-7. Cancer Genet Cytogenet. 2002. PMID: 12034532

4

Mosaicism in Prader-Willi syndrome.

Mowery-Rushton PA, Hanchett JM, Zipf WB, Rogan PK, Surti U. Mowery-Rushton PA, et al. Am J Med Genet. 2000 Jan 17;90(2):177. Am J Med Genet. 2000. PMID: 10722401 No abstract available.

5

Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28.

Pegoraro E, Whitaker J, Mowery-Rushton P, Surti U, Lanasa M, Hoffman EP. Pegoraro E, et al. Among authors: mowery rushton p. Am J Hum Genet. 1997 Jul;61(1):160-70. doi: 10.1086/513901. Am J Hum Genet. 1997. PMID: 9245997 Free PMC article.

6

Translocation (16;20)(p11.2;q13). sole cytogenetic abnormality in a unicameral bone cyst.

Richkind KE, Mortimer E, Mowery-Rushton P, Fraire A. Richkind KE, et al. Among authors: mowery rushton p. Cancer Genet Cytogenet. 2002 Sep;137(2):153-5. doi: 10.1016/s0165-4608(02)00563-0. Cancer Genet Cytogenet. 2002. PMID: 12393289

7

Translocation (3;12)(q25;p11.2): a recurrent cytogenetic abnormality in acute myeloid leukemia.

Shah R, Rowland B, Richkind K, Mowery-Rushton P, Roherty S, Morgan R, Schlam M. Shah R, et al. Among authors: mowery rushton p. Cancer Genet Cytogenet. 2005 Jan 15;156(2):186-7. doi: 10.1016/j.cancergencyto.2004.04.010. Cancer Genet Cytogenet. 2005. PMID: 15642404 No abstract available.

8

Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s.

Wenger SL, Boone LY, Cummins JH, Del Vecchio MA, Bay CA, Hummel M, Mowery-Rushton PA. Wenger SL, et al. Among authors: mowery rushton pa. Am J Med Genet. 2000 Apr 24;91(5):351-4. Am J Med Genet. 2000. PMID: 10766997

9

Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features.

Estop AM, Mowery-Rushton PA, Cieply KM, Kochmar SJ, Sherer CR, Clemens M, Surti U, McPherson E. Estop AM, et al. Among authors: mowery rushton pa. J Med Genet. 1995 Oct;32(10):819-22. doi: 10.1136/jmg.32.10.819. J Med Genet. 1995. PMID: 8558564 Free PMC article.

10

Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.

Clemens M, Martsolf JT, Rogers JG, Mowery-Rushton P, Surti U, McPherson E. Clemens M, et al. Among authors: mowery rushton p. Am J Med Genet. 1996 Dec 2;66(1):95-100. doi: 10.1002/(SICI)1096-8628(19961202)66:1<95::AID-AJMG26>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8957524

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