Ledbetter DH - Search Results

1

A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.

Blouin JL, Christie DH, Gos A, Lynn A, Morris MA, Ledbetter DH, Chakravarti A, Antonarakis SE. Blouin JL, et al. Among authors: ledbetter dh. Am J Hum Genet. 1995 Aug;57(2):388-94. Am J Hum Genet. 1995. PMID: 7668265 Free PMC article.

2

Nondisjunction of chromosome 15: origin and recombination.

Robinson WP, Bernasconi F, Mutirangura A, Ledbetter DH, Langlois S, Malcolm S, Morris MA, Schinzel AA. Robinson WP, et al. Among authors: ledbetter dh. Am J Hum Genet. 1993 Sep;53(3):740-51. Am J Hum Genet. 1993. PMID: 8352279 Free PMC article.

3

Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.

Patel PI, Franco B, Garcia C, Slaugenhaupt SA, Nakamura Y, Ledbetter DH, Chakravarti A, Lupski JR. Patel PI, et al. Among authors: ledbetter dh. Am J Hum Genet. 1990 Apr;46(4):801-9. Am J Hum Genet. 1990. PMID: 2316525 Free PMC article.

4

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.

Christian SL, Robinson WP, Huang B, Mutirangura A, Line MR, Nakao M, Surti U, Chakravarti A, Ledbetter DH. Christian SL, et al. Among authors: ledbetter dh. Am J Hum Genet. 1995 Jul;57(1):40-8. Am J Hum Genet. 1995. PMID: 7611294 Free PMC article.

5

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Mutirangura A, Greenberg F, Butler MG, Malcolm S, Nicholls RD, Chakravarti A, Ledbetter DH. Mutirangura A, et al. Among authors: ledbetter dh. Hum Mol Genet. 1993 Feb;2(2):143-51. doi: 10.1093/hmg/2.2.143. Hum Mol Genet. 1993. PMID: 8499903 Free PMC article.

6

A somatic cell hybrid map of human chromosome 13.

Washington SS, Bowcock AM, Gerken S, Matsunami N, Lesh D, Osborne-Lawrence SL, Cowell J, Ledbetter DH, White RL, Chakravarti A. Washington SS, et al. Among authors: ledbetter dh. Genomics. 1993 Dec;18(3):486-95. doi: 10.1016/s0888-7543(11)80004-2. Genomics. 1993. PMID: 8307557

7

Determination of the origin of nondisjunction in a 49,XXXXY male using hypervariable dinucleotide repeat sequences.

Huang TH, Greenberg F, Ledbetter DH. Huang TH, et al. Among authors: ledbetter dh. Hum Genet. 1991 Apr;86(6):619-20. doi: 10.1007/BF00201553. Hum Genet. 1991. PMID: 2026425

8

New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.

Schnur RE, Ledbetter SA, Ledbetter DH, Merry DE, Nussbaum RL. Schnur RE, et al. Among authors: ledbetter dh, ledbetter sa. Am J Hum Genet. 1989 Feb;44(2):248-54. Am J Hum Genet. 1989. PMID: 2563194 Free PMC article.

9

Dinucleotide repeat polymorphism mapping to the critical region for lissencephaly (17p13.3).

Carrozzo R, Ledbetter DH. Carrozzo R, et al. Among authors: ledbetter dh. Hum Mol Genet. 1993 May;2(5):615. doi: 10.1093/hmg/2.5.615. Hum Mol Genet. 1993. PMID: 8518813 No abstract available.

10

Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).

Huang TH, Hejtmancik JF, Edwards A, Pettigrew AL, Herrera CA, Hammond HA, Caskey CT, Zoghbi HY, Ledbetter DH. Huang TH, et al. Among authors: ledbetter dh. Am J Hum Genet. 1991 Dec;49(6):1312-9. Am J Hum Genet. 1991. PMID: 1746558 Free PMC article.

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