Loesch DZ - Search Results

1

FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 alleles.

Godler DE, Slater HR, Bui QM, Ono M, Gehling F, Francis D, Amor DJ, Hopper JL, Hagerman R, Loesch DZ. Godler DE, et al. Among authors: loesch dz. J Mol Diagn. 2011 Sep;13(5):528-36. doi: 10.1016/j.jmoldx.2011.05.006. Epub 2011 Jun 30. J Mol Diagn. 2011. PMID: 21723415 Free PMC article.

2

Timing and genetic rapport between growth in skeletal maturity and height around puberty: similarities and differences between girls and boys.

Loesch DZ, Hopper JL, Rogucka E, Huggins RM. Loesch DZ, et al. Am J Hum Genet. 1995 Mar;56(3):753-9. Am J Hum Genet. 1995. PMID: 7887431 Free PMC article.

3

Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring.

Loesch DZ, Huggins R, Petrovic V, Slater H. Loesch DZ, et al. Am J Hum Genet. 1995 Dec;57(6):1408-13. Am J Hum Genet. 1995. PMID: 8533771 Free PMC article.

4

Genetic correlates of menarcheal age: a multivariate twin study.

Loesch DZ, Huggins R, Rogucka E, Hoang NH, Hopper JL. Loesch DZ, et al. Ann Hum Biol. 1995 Nov-Dec;22(6):470-90. doi: 10.1080/03014469500004152. Ann Hum Biol. 1995. PMID: 8815776 Free article.

5

"Reduction" of CGG trinucleotide expansion from mother to offspring in seven fragile-X families.

Loesch DZ, Petrovic V, Francis DI, Oertel R, Slater H. Loesch DZ, et al. Clin Genet. 1997 Jan;51(1):1-6. doi: 10.1111/j.1399-0004.1997.tb02405.x. Clin Genet. 1997. PMID: 9084926

6

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: loesch dz. Am J Med Genet. 2000 Sep 18;94(3):232-6. doi: 10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10995510

7

Melatonin profiles and sleep characteristics in boys with fragile X syndrome: a preliminary study.

Gould EL, Loesch DZ, Martin MJ, Hagerman RJ, Armstrong SM, Huggins RM. Gould EL, et al. Among authors: loesch dz. Am J Med Genet. 2000 Dec 11;95(4):307-15. Am J Med Genet. 2000. PMID: 11186882

8

Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis.

Loesch DZ, Huggins RM, Bui QM, Epstein JL, Taylor AK, Hagerman RJ. Loesch DZ, et al. J Dev Behav Pediatr. 2002 Dec;23(6):416-23. doi: 10.1097/00004703-200212000-00004. J Dev Behav Pediatr. 2002. PMID: 12476071

9

Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspective.

Loesch DZ, Huggins RM, Bui QM, Taylor AK, Hagerman RJ. Loesch DZ, et al. Am J Med Genet A. 2003 Apr 15;118A(2):127-34. doi: 10.1002/ajmg.a.10099. Am J Med Genet A. 2003. PMID: 12655493

10

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis.

Loesch DZ, Huggins RM, Bui QM, Taylor AK, Pratt C, Epstein J, Hagerman RJ. Loesch DZ, et al. Am J Med Genet A. 2003 Sep 15;122A(1):13-23. doi: 10.1002/ajmg.a.20214. Am J Med Genet A. 2003. PMID: 12949966

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