Hu L - Search Results

1

Evidence against a major role of PEG1/MEST in Silver-Russell syndrome.

Riesewijk AM, Blagitko N, Schinzel AA, Hu L, Schulz U, Hamel BC, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: hu l. Eur J Hum Genet. 1998 Mar-Apr;6(2):114-20. doi: 10.1038/sj.ejhg.5200164. Eur J Hum Genet. 1998. PMID: 9781054

2

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses.

Riesewijk AM, Hu L, Schulz U, Tariverdian G, Höglund P, Kere J, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: hu l. Genomics. 1997 Jun 1;42(2):236-44. doi: 10.1006/geno.1997.4731. Genomics. 1997. PMID: 9192843 Free article.

3

Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4.

de Kok YJ, Vossenaar ER, Cremers CW, Dahl N, Laporte J, Hu LJ, Lacombe D, Fischel-Ghodsian N, Friedman RA, Parnes LS, Thorpe P, Bitner-Glindzicz M, Pander HJ, Heilbronner H, Graveline J, den Dunnen JT, Brunner HG, Ropers HH, Cremers FP. de Kok YJ, et al. Among authors: hu lj. Hum Mol Genet. 1996 Sep;5(9):1229-35. doi: 10.1093/hmg/5.9.1229. Hum Mol Genet. 1996. PMID: 8872461

4

Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathy.

Laporte J, Guiraud-Chaumeil C, Tanner SM, Blondeau F, Hu LJ, Vicaire S, Liechti-Gallati S, Mandel JL. Laporte J, et al. Among authors: hu lj. Eur J Hum Genet. 1998 Jul-Aug;6(4):325-30. doi: 10.1038/sj.ejhg.5200189. Eur J Hum Genet. 1998. PMID: 9781038

5

X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markers.

Hu LJ, Laporte J, Kioschis P, Heyberger S, Kretz C, Poustka A, Mandel JL, Dahi N. Hu LJ, et al. Hum Genet. 1996 Aug;98(2):178-81. doi: 10.1007/s004390050185. Hum Genet. 1996. PMID: 8698337

6

Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region.

Hu LJ, Laporte J, Kress W, Kioschis P, Siebenhaar R, Poustka A, Fardeau M, Metzenberg A, Janssen EA, Thomas N, Mandel JL, Dahl N. Hu LJ, et al. Hum Mol Genet. 1996 Jan;5(1):139-43. doi: 10.1093/hmg/5.1.139. Hum Mol Genet. 1996. PMID: 8789451

7

Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.

Dahl N, Hu LJ, Chery M, Fardeau M, Gilgenkrantz S, Nivelon-Chevallier A, Sidaner-Noisette I, Mugneret F, Gouyon JB, Gal A, et al. Dahl N, et al. Among authors: hu lj. Am J Hum Genet. 1995 May;56(5):1108-15. Am J Hum Genet. 1995. PMID: 7726166 Free PMC article.

8

Dinucleotide repeat polymorphism at the DXS1684 locus.

Gong W, Hu L, Kioschis P, Poutska A, Dahl N. Gong W, et al. Among authors: hu l. Hum Mol Genet. 1994 Aug;3(8):1442. doi: 10.1093/hmg/3.8.1442. Hum Mol Genet. 1994. PMID: 7987337 No abstract available.

9

Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26.

Dahl N, Laporte J, Hu L, Biancalana V, Le Palier D, Cohen D, Piussan C, Mandel JL. Dahl N, et al. Among authors: hu l. Am J Hum Genet. 1995 Apr;56(4):999-1002. Am J Hum Genet. 1995. PMID: 7717411 Free PMC article. No abstract available.

10

Causality research based on phase space reconstruction.

Hu L, Sunu Z, She H, Fan B, Ma J, Da C. Hu L, et al. PLoS One. 2024 Nov 22;19(11):e0313990. doi: 10.1371/journal.pone.0313990. eCollection 2024. PLoS One. 2024. PMID: 39576828

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