Micale MA - Search Results

1

Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

Christ LA, Crowe CA, Micale MA, Conroy JM, Schwartz S. Christ LA, et al. Among authors: micale ma. Am J Hum Genet. 1999 Nov;65(5):1387-95. doi: 10.1086/302606. Am J Hum Genet. 1999. PMID: 10521304 Free PMC article.

2

Parental origin of De Novo chromosome 9 deletions in del(9p) syndrome.

Micale MA, Haren JM, Conroy JM, Crowe CA, Schwartz S. Micale MA, et al. Am J Med Genet. 1995 May 22;57(1):79-81. doi: 10.1002/ajmg.1320570118. Am J Med Genet. 1995. PMID: 7645605

3

Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.

Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S. Micale MA, et al. Prenat Diagn. 1996 Oct;16(10):893-7. doi: 10.1002/(SICI)1097-0223(199610)16:10<893::AID-PD962>3.0.CO;2-M. Prenat Diagn. 1996. PMID: 8938057

4

Preparation of amniocytes for interphase fluorescence in situ hybridization (FISH).

Schwartz S, Micale MA, Becker L. Schwartz S, et al. Among authors: micale ma. Curr Protoc Hum Genet. 2001 May;Chapter 8:Unit 8.9. doi: 10.1002/0471142905.hg0809s05. Curr Protoc Hum Genet. 2001. PMID: 18428317

5

A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes.

Dewald G, Stallard R, Al Saadi A, Arnold S, Bader PI, Blough R, Chen K, Elejalde BR, Harris CJ, Higgins RR, Hoeltge GA, Hsu WT, Kubic V, McCorquodale DJ, Micale MA, Moore JW, Phillips RM, Scheib-Wixted S, Schwartz S, Siembieda S, Strole K, VanTuinen P, Vance GH, Wiktor A, Zinsmeister A, et al. Dewald G, et al. Among authors: micale ma. Am J Med Genet. 1998 Apr 1;76(4):318-26. Am J Med Genet. 1998. PMID: 9545096

6

A multicenter investigation with D-FISH BCR/ABL1 probes.

Dewald G, Stallard R, Alsaadi A, Arnold S, Blough R, Ceperich TM, Rafael Elejalde B, Fink J, Higgins JV, Higgins RR, Hoeltge GA, Hsu WT, Johnson EB, Kronberger D, McCorquodale DJ, Meisner LF, Micale MA, Oseth L, Payne JS, Schwartz S, Sheldon S, Sophian A, Storto P, Van Tuinen P, Wenger GD, Wiktor A, Willis LA, Yung JF, Zenger-Hain J. Dewald G, et al. Among authors: micale ma. Cancer Genet Cytogenet. 2000 Jan 15;116(2):97-104. doi: 10.1016/s0165-4608(99)00120-x. Cancer Genet Cytogenet. 2000. PMID: 10640140 Clinical Trial.

7

Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1-q24.2 contiguous gene deletion.

Seeley AH, Durham MA, Micale MA, Wesolowski J, Foerster BR, Martin DM. Seeley AH, et al. Among authors: micale ma. Am J Med Genet A. 2014 Aug;164A(8):2062-8. doi: 10.1002/ajmg.a.36569. Epub 2014 Apr 9. Am J Med Genet A. 2014. PMID: 24719385 Free PMC article.

8

Defining the extent and nature of cytogenetic events in prostatic adenocarcinoma: paraffin FISH vs. metaphase analysis.

Micale MA, Sanford JS, Powell IJ, Sakr WA, Wolman SR. Micale MA, et al. Cancer Genet Cytogenet. 1993 Aug;69(1):7-12. doi: 10.1016/0165-4608(93)90103-s. Cancer Genet Cytogenet. 1993. PMID: 8374904

9

Chromosomal aneuploidy in proliferative breast disease.

Micale MA, Visscher DW, Gulino SE, Wolman SR. Micale MA, et al. Hum Pathol. 1994 Jan;25(1):29-35. doi: 10.1016/0046-8177(94)90167-8. Hum Pathol. 1994. PMID: 8314258

10

Mosaic variegated aneuploidy without microcephaly: implications for cytogenetic diagnosis.

Micale MA, Schran D, Emch S, Kurczynski TW, Rahman N, Van Dyke DL. Micale MA, et al. Am J Med Genet A. 2007 Aug 15;143A(16):1890-3. doi: 10.1002/ajmg.a.31848. Am J Med Genet A. 2007. PMID: 17632782

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