Kjellberg P - Search Results

1

[DNA amplification in the study of polymorphisms linked to the cystic fibrosis gene].

Claustres M, Bellet H, Desgeorges M, Kjellberg P, Toueri MF, Rollin B, Bonnet H. Claustres M, et al. Among authors: kjellberg p. J Genet Hum. 1989 Sep;37(3):243-9. J Genet Hum. 1989. PMID: 2576281 French.

2

[Detection of deletions by the amplification of exons (multiplex PCR) in Duchenne muscular dystrophy].

Claustres M, Kjellberg P, Desgeorges M, Bellet H, Sarda P, Bonnet H, Boileau C. Claustres M, et al. Among authors: kjellberg p. J Genet Hum. 1989 Sep;37(3):251-7. J Genet Hum. 1989. PMID: 2625628 French.

3

Analysis of 30 known cystic fibrosis mutations: 10 mutations account for 27% of non-delta F508 chromosomes in southern France.

Claustres M, Desgeorges M, Kjellberg P, Tissot C, Demaille J. Claustres M, et al. Among authors: kjellberg p. Hum Genet. 1992 Dec;90(4):464-6. doi: 10.1007/BF00220479. Hum Genet. 1992. PMID: 1483707

4

Cystic fibrosis typing with DNA probes and screening for delta F508 deletion in families from southern France.

Claustres M, Desgeorges M, Kjellberg P, Bellet H, Demaille J, Ramsay M. Claustres M, et al. Among authors: kjellberg p. Hum Genet. 1990 Sep;85(4):398-9. doi: 10.1007/BF02428274. Hum Genet. 1990. PMID: 1976591

5

Identification of carriers by screening for delta F508 deletion in a multi-generation cystic fibrosis family.

Claustres M, Desgeorges M, Kjellberg P, Demaille J. Claustres M, et al. Among authors: kjellberg p. Genet Couns. 1990;1(3-4):211-7. Genet Couns. 1990. PMID: 1982988

6

A healthy male with compound and double heterozygosities for delta F508, F508C, and M47OV in exon 10 of the cystic fibrosis gene.

Desgeorges M, Kjellberg P, Demaille J, Claustres M. Desgeorges M, et al. Among authors: kjellberg p. Am J Hum Genet. 1994 Feb;54(2):384-5. Am J Hum Genet. 1994. PMID: 7508183 Free PMC article. No abstract available.

7

Prenatal diagnosis for cystic fibrosis using SSCP analysis.

Desgeorges M, Boulot P, Kjellberg P, Lefort G, Rolland M, Demaille J, Claustres M. Desgeorges M, et al. Among authors: kjellberg p. Prenat Diagn. 1993 Feb;13(2):147-8. doi: 10.1002/pd.1970130211. Prenat Diagn. 1993. PMID: 7681978 No abstract available.

8

Screening for cystic fibrosis mutations in southern France: identification of a frameshift mutation and two missense variations.

Claustres M, Gerrard B, Kjellberg P, Desgeorges M, Demaille J, Dean M. Claustres M, et al. Among authors: kjellberg p. Hum Mutat. 1992;1(4):310-3. doi: 10.1002/humu.1380010408. Hum Mutat. 1992. PMID: 1284537

9

A new mutation (1078delT) in exon 7 of the CFTR gene in a southern French adult with cystic fibrosis.

Claustres M, Gerrard B, White MB, Desgeorges M, Kjellberg P, Rollin B, Dean M. Claustres M, et al. Among authors: kjellberg p. Genomics. 1992 Jul;13(3):907-8. doi: 10.1016/0888-7543(92)90187-w. Genomics. 1992. PMID: 1379211 No abstract available.

10

Germinal mosaicism from grand-paternal origin in a family with Duchenne muscular dystrophy.

Claustres M, Kjellberg P, Desgeorges M, Bellet H, Demaille J. Claustres M, et al. Among authors: kjellberg p. Hum Genet. 1990 Dec;86(2):241-3. doi: 10.1007/BF00197714. Hum Genet. 1990. PMID: 1979959

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