Loeb D - Search Results

1

Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.

Othmane KB, Loeb D, Hayworth-Hodgte R, Hentati F, Rao N, Roses AD, Ben Hamida M, Pericak-Vance MA, Vance JM. Othmane KB, et al. Among authors: loeb d. Genomics. 1995 Jul 20;28(2):286-90. doi: 10.1006/geno.1995.1143. Genomics. 1995. PMID: 8530038

2

A novel mutation in the von Hippel-Lindau gene.

Loeb DB, Pericak-Vance MA, Stajich JM, Vance JM. Loeb DB, et al. Hum Mol Genet. 1994 Aug;3(8):1423-4. doi: 10.1093/hmg/3.8.1423. Hum Mol Genet. 1994. PMID: 7987327 No abstract available.

3

Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellites.

Denton PH, Cullen JB, Loeb D, Lucas A, Nunes K, Hulett C, Vance JM. Denton PH, et al. Among authors: loeb d. Nucleic Acids Res. 1994 May 11;22(9):1776-7. doi: 10.1093/nar/22.9.1776. Nucleic Acids Res. 1994. PMID: 8202390 Free PMC article.

4

Dinucleotide repeat polymorphism in the VHL region.

Loeb D, Lui W, Smith DI, Vance JM. Loeb D, et al. Hum Mol Genet. 1994 Mar;3(3):520. doi: 10.1093/hmg/3.3.520. Hum Mol Genet. 1994. PMID: 8012368 No abstract available.

5

Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.

Pericak-Vance MA, Nunes KJ, Whisenant E, Loeb DB, Small KW, Stajich JM, Rimmler JB, Yamaoka LH, Smith DI, Drabkin HA, et al. Pericak-Vance MA, et al. Among authors: loeb db. J Med Genet. 1993 Jun;30(6):487-91. doi: 10.1136/jmg.30.6.487. J Med Genet. 1993. PMID: 8100855 Free PMC article.

6

Dinucleotide repeat polymorphisms in the VHL region of human chromosome 3p25.

Loeb D, Lui W, Smith DI, Vance JM. Loeb D, et al. Hum Mol Genet. 1993 Oct;2(10):1746. doi: 10.1093/hmg/2.10.1746. Hum Mol Genet. 1993. PMID: 8268940 No abstract available.

7

Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C).

Ben Othmane K, Speer MC, Stauffer J, Blel S, Middleton L, Ben Hamida C, Etribi A, Loeb D, Hentati F, Roses AD, et al. Ben Othmane K, et al. Among authors: loeb d. Am J Hum Genet. 1995 Sep;57(3):732-4. Am J Hum Genet. 1995. PMID: 7668303 Free PMC article. No abstract available.

8

Dinucleotide repeats flanking the renal carcinoma breakpoint at 3p14.2.

Roche J, Whisenant E, Boldog F, Loeb D, Vance JM, Drabkin H. Roche J, et al. Among authors: loeb d. Hum Mol Genet. 1994 Jan;3(1):215. doi: 10.1093/hmg/3.1.215. Hum Mol Genet. 1994. PMID: 8162042 No abstract available.

9

A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene region.

Thomas W, Fullan A, Loeb DB, McClelland EE, Bacon BR, Wolff RK. Thomas W, et al. Among authors: loeb db. Hum Genet. 1998 May;102(5):517-25. doi: 10.1007/s004390050734. Hum Genet. 1998. PMID: 9654199

10

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.

Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R Jr, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Risch NJ, Bacon BR, Wolff RK. Feder JN, et al. Among authors: loeb db. Nat Genet. 1996 Aug;13(4):399-408. doi: 10.1038/ng0896-399. Nat Genet. 1996. PMID: 8696333

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