Marlhens F - Search Results

1

De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.

Chelly J, Marlhens F, Le Marec B, Jeanpierre M, Lambert M, Hamard G, Dutrillaux B, Kaplan JC. Chelly J, et al. Among authors: marlhens f. Hum Genet. 1986 Oct;74(2):193-6. doi: 10.1007/BF00282093. Hum Genet. 1986. PMID: 2876949

2

The rate of chromosome breakage is age dependent in lymphocytes of adult controls.

Marlhens F, Achkar WA, Aurias A, Couturier J, Dutrillaux AM, Gerbault-Sereau M, Hoffschir F, Lamoliatte E, Lefrançois D, Lombard M, et al. Marlhens F, et al. Hum Genet. 1986 Aug;73(4):290-7. doi: 10.1007/BF00279088. Hum Genet. 1986. PMID: 3744361

3

Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality.

Huret JL, Delabar JM, Marlhens F, Aurias A, Nicole A, Berthier M, Tanzer J, Sinet PM. Huret JL, et al. Among authors: marlhens f. Hum Genet. 1987 Mar;75(3):251-7. doi: 10.1007/BF00281069. Hum Genet. 1987. PMID: 2951317

4

Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia.

Chelly J, Marlhens F, Dutrillaux B, Van Ommen GJ, Lambert M, Haioun B, Boissinot G, Fardeau M, Kaplan JC. Chelly J, et al. Among authors: marlhens f. Hum Genet. 1988 Mar;78(3):222-7. doi: 10.1007/BF00291665. Hum Genet. 1988. PMID: 2894344

5

Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probe.

Delattre O, Bernard A, Malfoy B, Marlhens F, Viegas-Pequignot E, Brossard C, Haguenauer O, Creau-Goldberg N, N'guyen VC, Dutrillaux B, et al. Delattre O, et al. Among authors: marlhens f. Hum Hered. 1988;38(3):156-67. doi: 10.1159/000153777. Hum Hered. 1988. PMID: 2899543

6

Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia.

Marlhens F, Chelly J, Kaplan JC, Lefrancois D, Harpey JP, Dutrillaux B. Marlhens F, et al. Hum Genet. 1987 Dec;77(4):379-83. doi: 10.1007/BF00291430. Hum Genet. 1987. PMID: 2891606

7

Isolation and characterization of an alphoid DNA sequence recently amplified on human chromosome 3.

Delattre O, Bernard A, Malfoy B, Marlhens F, Viegas-Pequignot E, Brossard C, Haguenauer O, Creau-Goldberg N, Van Cong N, Dutrillaux B, et al. Delattre O, et al. Among authors: marlhens f. Nucleic Acids Res. 1987 Oct 26;15(20):8561. Nucleic Acids Res. 1987. PMID: 3671092 Free PMC article. No abstract available.

8

Karyotype evolution of the human HBL-100 cell line and mapping of the integration site of SV40 DNA.

Marlhens F, Saint-Ruf C, Nardeux P, Lavialle C, Brouty-Boye D, Dutrillaux B, Cassingena R. Marlhens F, et al. Ann Genet. 1988;31(2):81-6. Ann Genet. 1988. PMID: 2840847

9

Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene.

Marlhens F, Griffoin JM, Bareil C, Arnaud B, Claustres M, Hamel CP. Marlhens F, et al. Eur J Hum Genet. 1998 Sep-Oct;6(5):527-31. doi: 10.1038/sj.ejhg.5200205. Eur J Hum Genet. 1998. PMID: 9801879

10

RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8).

Marlhens F, Delattre O, Bernard A, Olschwang S, Dutrillaux B, Thomas G. Marlhens F, et al. Nucleic Acids Res. 1987 Feb 11;15(3):1348. doi: 10.1093/nar/15.3.1348. Nucleic Acids Res. 1987. PMID: 2434930 Free PMC article. No abstract available.

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