Milunsky A - Search Results

1

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

Skare J, Milunsky J, Milunsky A. Skare J, et al. Among authors: milunsky a, milunsky j. 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.

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

Interstitial deletion involving most of Yq.

Skare J, Drwinga H, Wyandt H, vanderSpek J, Troxler R, Milunsky A. Skare J, et al. Among authors: milunsky a. Am J Med Genet. 1990 Aug;36(4):394-7. doi: 10.1002/ajmg.1320360405. Am J Med Genet. 1990. PMID: 2389795

4

Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq.

Skare JC, Sullivan JL, Milunsky A. Skare JC, et al. Among authors: milunsky a. Hum Genet. 1989 Jul;82(4):349-53. doi: 10.1007/BF00273996. Hum Genet. 1989. PMID: 2567695

5

Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37.

Skare JC, Grierson HL, Sullivan JL, Nussbaum RL, Purtilo DT, Sylla BS, Lenoir GM, Reilly DS, White BN, Milunsky A. Skare JC, et al. Among authors: milunsky a. Hum Genet. 1989 Jul;82(4):354-8. doi: 10.1007/BF00273997. Hum Genet. 1989. PMID: 2567696

6

A new mutation causing familial amyloidotic polyneuropathy.

Skare JC, Saraiva MJ, Alves IL, Skare IB, Milunsky A, Cohen AS, Skinner M. Skare JC, et al. Among authors: milunsky a. Biochem Biophys Res Commun. 1989 Nov 15;164(3):1240-6. doi: 10.1016/0006-291x(89)91802-0. Biochem Biophys Res Commun. 1989. PMID: 2590199 Free article.

7

Localization of the genes for histatins to human chromosome 4q13 and tissue distribution of the mRNAs.

vanderSpek JC, Wyandt HE, Skare JC, Milunsky A, Oppenheim FG, Troxler RF. vanderSpek JC, et al. Among authors: milunsky a. Am J Hum Genet. 1989 Sep;45(3):381-7. Am J Hum Genet. 1989. PMID: 2773933 Free PMC article.

8

Localization of the gene for human heart fatty acid binding protein to chromosome 1p32-1p33.

Troxler RF, Offner GD, Jiang JW, Wu BL, Skare JC, Milunsky A, Wyandt HE. Troxler RF, et al. Among authors: milunsky a. Hum Genet. 1993 Dec;92(6):563-6. doi: 10.1007/BF00420939. Hum Genet. 1993. PMID: 8262516

9

Familial supernumerary chromosome and malignancy.

Milunsky JM, Wyandt HE, Milunsky A. Milunsky JM, et al. Among authors: milunsky a. Cancer Genet Cytogenet. 1996 Jul 15;89(2):170-2. doi: 10.1016/0165-4608(96)00069-6. Cancer Genet Cytogenet. 1996. PMID: 8697427 Free article.

10

Schizophrenia susceptibility gene locus at Xp22.3.

Milunsky J, Huang XL, Wyandt HE, Milunsky A. Milunsky J, et al. Among authors: milunsky a. Clin Genet. 1999 Jun;55(6):455-60. doi: 10.1034/j.1399-0004.1999.550610.x. Clin Genet. 1999. PMID: 10450863

Patient 1 was previously reported by us (Wyandt HE, Bugeau-Michaud L, Skare JC, Milunsky A. Partial duplication of Xp: a case report and review of previously reported cases. ...Patient 2 is a 14-year-old girl with short stature, learning disabilities, …

Patient 1 was previously reported by us (Wyandt HE, Bugeau-Michaud L, Skare JC, Milunsky A. Partial duplication of Xp: a …

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