Milunsky JM - Search Results

1

Presymptomatic and prenatal diagnosis of myotonic muscular dystrophy with linked DNA probes.

Milunsky JM, Skare JC, Milunsky A. Milunsky JM, et al. Among authors: milunsky a. Am J Med Sci. 1991 Apr;301(4):231-7. doi: 10.1097/00000441-199104000-00001. Am J Med Sci. 1991. PMID: 1672791

2

Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probes.

Milunsky A, Skare JC, Milunsky JM, Maher TA, Amos JA. Milunsky A, et al. Among authors: milunsky jm. Am J Obstet Gynecol. 1991 Mar;164(3):751-5. doi: 10.1016/0002-9378(91)90509-p. Am J Obstet Gynecol. 1991. PMID: 2003536

3

Case report: cystic fibrosis and embryonal carcinoma of the testis.

Milunsky JM, Milunsky A. Milunsky JM, et al. Among authors: milunsky a. Am J Med Sci. 1996 Apr;311(4):191-2. doi: 10.1097/00000441-199604000-00009. Am J Med Sci. 1996. PMID: 8602651 Free article.

4

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

5

Precise prenatal diagnosis of tuberous sclerosis by sequencing the TSC2 gene.

Milunsky A, Shim SH, Ito M, Jaekle RK, Bassett LL, Brumund MR, Milunsky JM. Milunsky A, et al. Among authors: milunsky jm. Prenat Diagn. 2005 Jul;25(7):582-5. doi: 10.1002/pd.1197. Prenat Diagn. 2005. PMID: 16032769

6

L2, a DNA fragment from Xq24-q27, detects an EcoR1 RFLP (HGM9 no. DXS12).

Skare J, Milunsky J, Milunsky A. Skare J, et al. Nucleic Acids Res. 1989 Jun 26;17(12):4909. doi: 10.1093/nar/17.12.4909. Nucleic Acids Res. 1989. PMID: 2568617 Free PMC article.

7

Characterization of a duplication in the terminal band of 4p by molecular cytogenetics.

Wyandt HE, Milunsky J, Lerner T, Gusella JF, Hou A, MacDonald M, Adekunle S, Milunsky A. Wyandt HE, et al. Am J Med Genet. 1993 Apr 1;46(1):72-6. doi: 10.1002/ajmg.1320460112. Am J Med Genet. 1993. PMID: 7684190

8

Familial paragangliomas: linkage to chromosome 11q23 and clinical implications.

Milunsky J, DeStefano AL, Huang XL, Baldwin CT, Michels VV, Jako G, Milunsky A. Milunsky J, et al. Am J Med Genet. 1997 Oct 3;72(1):66-70. doi: 10.1002/(sici)1096-8628(19971003)72:1<66::aid-ajmg14>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9295078

9

Prenatal diagnosis for Schmid metaphyseal chondrodysplasia in twins.

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

10

A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90.

Skare JC, Milunsky JM, Milunsky A, Skare IB, Cohen AS, Skinner M. Skare JC, et al. Among authors: milunsky a, milunsky jm. Clin Genet. 1991 Jan;39(1):6-12. doi: 10.1111/j.1399-0004.1991.tb02979.x. Clin Genet. 1991. PMID: 1997217

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