Kretz C - Search Results

1

A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast.

Laporte J, Hu LJ, Kretz C, Mandel JL, Kioschis P, Coy JF, Klauck SM, Poustka A, Dahl N. Laporte J, et al. Among authors: kretz c. Nat Genet. 1996 Jun;13(2):175-82. doi: 10.1038/ng0696-175. Nat Genet. 1996. PMID: 8640223

2

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.

Heitz D, Devys D, Imbert G, Kretz C, Mandel JL. Heitz D, et al. Among authors: kretz c. J Med Genet. 1992 Nov;29(11):794-801. doi: 10.1136/jmg.29.11.794. J Med Genet. 1992. PMID: 1453430 Free PMC article.

3

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.

Vincent A, Heitz D, Petit C, Kretz C, Oberlé I, Mandel JL. Vincent A, et al. Among authors: kretz c. Nature. 1991 Feb 14;349(6310):624-6. doi: 10.1038/349624a0. Nature. 1991. PMID: 1672039

4

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.

Oberlé I, Rousseau F, Heitz D, Kretz C, Devys D, Hanauer A, Boué J, Bertheas MF, Mandel JL. Oberlé I, et al. Among authors: kretz c. Science. 1991 May 24;252(5009):1097-102. doi: 10.1126/science.252.5009.1097. Science. 1991. PMID: 2031184

5

A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

Vincent A, Kretz C, Oberlé I, Mandel JL. Vincent A, et al. Among authors: kretz c. Hum Genet. 1989 Apr;82(1):85-6. doi: 10.1007/BF00288280. Hum Genet. 1989. PMID: 2565870

6

Genomic organization of the adrenoleukodystrophy gene.

Sarde CO, Mosser J, Kioschis P, Kretz C, Vicaire S, Aubourg P, Poustka A, Mandel JL. Sarde CO, et al. Among authors: kretz c. Genomics. 1994 Jul 1;22(1):13-20. doi: 10.1006/geno.1994.1339. Genomics. 1994. PMID: 7959759

7

The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein.

Mosser J, Lutz Y, Stoeckel ME, Sarde CO, Kretz C, Douar AM, Lopez J, Aubourg P, Mandel JL. Mosser J, et al. Among authors: kretz c. Hum Mol Genet. 1994 Feb;3(2):265-71. doi: 10.1093/hmg/3.2.265. Hum Mol Genet. 1994. PMID: 8004093

8

Origin of the expansion mutation in myotonic dystrophy.

Imbert G, Kretz C, Johnson K, Mandel JL. Imbert G, et al. Among authors: kretz c. Nat Genet. 1993 May;4(1):72-6. doi: 10.1038/ng0593-72. Nat Genet. 1993. PMID: 8513329

9

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. Among authors: kretz c. Hum Genet. 1996 Aug;98(2):178-81. doi: 10.1007/s004390050185. Hum Genet. 1996. PMID: 8698337

10

Cloning and characterization of an alternatively spliced gene in proximal Xq28 deleted in two patients with intersexual genitalia and myotubular myopathy.

Laporte J, Kioschis P, Hu LJ, Kretz C, Carlsson B, Poustka A, Mandel JL, Dahl N. Laporte J, et al. Among authors: kretz c. Genomics. 1997 May 1;41(3):458-62. doi: 10.1006/geno.1997.4662. Genomics. 1997. PMID: 9169146

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

103 results

Search Page

Filters