Carpenter NJ - Search Results

1

Genetic anticipation. Expanding tandem repeats.

Carpenter NJ. Carpenter NJ. Neurol Clin. 1994 Nov;12(4):683-97. Neurol Clin. 1994. PMID: 7845337 Review.

2

Technical pitfalls encountered in PCR quantification using microsatellites.

Qu Y, Whetsell L, Carpenter NJ. Qu Y, et al. Among authors: carpenter nj. Genet Test. 1997-1998;1(3):213-5. doi: 10.1089/gte.1997.1.213. Genet Test. 1997. PMID: 10464648

3

Molecular cytogenetics.

Carpenter NJ. Carpenter NJ. Semin Pediatr Neurol. 2001 Sep;8(3):135-46. doi: 10.1053/spen.2001.26447. Semin Pediatr Neurol. 2001. PMID: 11575843 Review.

4

Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2.

Carpenter NJ, Brown WT, Qu Y, Keenan KL. Carpenter NJ, et al. Am J Med Genet. 1999 Jul 30;85(3):266-70. doi: 10.1002/(sici)1096-8628(19990730)85:3<266::aid-ajmg16>3.0.co;2-p. Am J Med Genet. 1999. PMID: 10398241

5

DNA linkage analysis of 26 families with fragile X syndrome.

Carpenter NJ. Carpenter NJ. Am J Med Genet. 1991 Feb-Mar;38(2-3):311-8. doi: 10.1002/ajmg.1320380229. Am J Med Genet. 1991. PMID: 1673303

6

X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq.

Carpenter NJ, Qu Y, Curtis M, Patil SR. Carpenter NJ, et al. Am J Med Genet. 1999 Jul 30;85(3):230-5. doi: 10.1002/(sici)1096-8628(19990730)85:3<230::aid-ajmg9>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10398234

7

Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus.

Carpenter NJ, Thibodeau SN, Brown WT. Carpenter NJ, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):349-53. doi: 10.1002/ajmg.1320380237. Am J Med Genet. 1991. PMID: 1673310

8

Linkage and risk assessment in fragile X families using new DNA probes at Xq27.

Carpenter NJ, Swartz-Boyd J, Prichard JK, Lam T. Carpenter NJ, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):312-9. doi: 10.1002/ajmg.1320430148. Am J Med Genet. 1992. PMID: 1351365

9

Charcot-Marie-Tooth disease type 1A: a family study with microsatellites.

Qu Y, Carpenter NJ, Whetsell L, Smith SP, Say B. Qu Y, et al. Among authors: carpenter nj. J Okla State Med Assoc. 1996 Nov;89(11):395-9. J Okla State Med Assoc. 1996. PMID: 8972170

10

Diagnosis of microdeletion syndromes: high-resolution chromosome analysis versus fluorescence in situ hybridization.

Gopal VV, Roop H, Carpenter NJ. Gopal VV, et al. Among authors: carpenter nj. Am J Med Sci. 1995 Apr;309(4):208-12. doi: 10.1097/00000441-199504000-00004. Am J Med Sci. 1995. PMID: 7900742 Clinical Trial.

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