Milunsky A - Search Results

1

Milunsky JM, Lebo RV, Ikuta T, Maher TA, Haverty CE, Milunsky A. Milunsky JM, et al. Among authors: milunsky a. Genet Test. 2001 Winter;5(4):321-5. doi: 10.1089/109065701753617462. Genet Test. 2001. PMID: 11960578

2

Gene sequencing in neonates and infants with the long QT syndrome.

Shim SH, Ito M, Maher T, Milunsky A. Shim SH, et al. Among authors: milunsky a. Genet Test. 2005 Winter;9(4):281-4. doi: 10.1089/gte.2005.9.281. Genet Test. 2005. PMID: 16379539

3

Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.

Milunsky JM, Maher TA, Michels VV, Milunsky A. Milunsky JM, et al. Among authors: milunsky a. Am J Med Genet. 2001 May 15;100(4):311-4. doi: 10.1002/ajmg.1270. Am J Med Genet. 2001. PMID: 11343322

4

Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region.

Lebo RV, Ikuta T, Milunsky JM, Milunsky A. Lebo RV, et al. Among authors: milunsky a, milunsky jm. Clin Genet. 2001 Jun;59(6):406-17. doi: 10.1034/j.1399-0004.2001.590605.x. Clin Genet. 2001. PMID: 11453972

5

The value of MLPA in Waardenburg syndrome.

Milunsky JM, Maher TA, Ito M, Milunsky A. Milunsky JM, et al. Among authors: milunsky a. Genet Test. 2007 Summer;11(2):179-82. doi: 10.1089/gte.2006.0531. Genet Test. 2007. PMID: 17627390

6

Genetic counseling in perinatal medicine.

Milunsky JM, Milunsky A. Milunsky JM, et al. Among authors: milunsky a. Obstet Gynecol Clin North Am. 1997 Mar;24(1):1-17. doi: 10.1016/s0889-8545(05)70286-2. Obstet Gynecol Clin North Am. 1997. PMID: 9086515 Free article. Review.

7

Prenatal diagnosis for Schmid metaphyseal chondrodysplasia in twins.

Milunsky J, Maher T, Lebo R, Milunsky A. Milunsky J, et al. Among authors: milunsky a. Fetal Diagn Ther. 1998 May-Jun;13(3):167-8. doi: 10.1159/000020831. Fetal Diagn Ther. 1998. PMID: 9708440

8

The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis.

Milunsky A, Konialis C, Shim SH, Maher TA, Spengos K, Ito M, Pangalos C. Milunsky A, et al. Prenat Diagn. 2005 Nov;25(11):1057-8. doi: 10.1002/pd.1302. Prenat Diagn. 2005. PMID: 16302168

9

Analysis by mass spectrometry of 100 cystic fibrosis gene mutations in 92 patients with congenital bilateral absence of the vas deferens.

Wang Z, Milunsky J, Yamin M, Maher T, Oates R, Milunsky A. Wang Z, et al. Among authors: milunsky a, milunsky j. Hum Reprod. 2002 Aug;17(8):2066-72. doi: 10.1093/humrep/17.8.2066. Hum Reprod. 2002. PMID: 12151438

10

Prenatal molecular diagnosis of tuberous sclerosis complex.

Milunsky A, Ito M, Maher TA, Flynn M, Milunsky JM. Milunsky A, et al. Among authors: milunsky jm. Am J Obstet Gynecol. 2009 Mar;200(3):321.e1-6. doi: 10.1016/j.ajog.2008.11.004. Am J Obstet Gynecol. 2009. PMID: 19254590

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