المؤلفون: Lucotte, G.^Aff4, Berriche, S.^Aff4, Pfitzinger, H.^Aff5, Ludes, B.^Aff5

المساهمون: Bär, Walter, editor^Aff1, Fiori, Angelo, editor^Aff2, Rossi, Umberto, editor^Aff3

المصدر: Advances in Forensic Haemogenetics : 15th Congress of the International Society for Forensic Haemogenetics (Internationale Gesellschaft für forensische Hämogenetik e.V.), Venezia, 13–15 October 1993. 5:530-532

المؤلفون: Petit, M. C., Francois, M. H., Berriche, S., Burckel, A., Lucotte, G.

المساهمون: Rolfs, Arndt, editor^Aff1, Schumacher, Hermann Christian, editor^Aff1, Marx, Peter, editor^Aff1

المصدر: PCR Topics : Usage of Polymerase Chain Reaction in Genetic and Infectious Diseases. :203-205

المؤلفون: Lucotte, G.^Aff3, Guérin, P.^Aff3, Berriche, S.^Aff3

المساهمون: Polesky, H. F., editor^Aff1, Mayr, Wolfgang R., editor^Aff2

المصدر: 13th Congress of the International Society for Forensic Haemogenetics (Internationale Gesellschaft für forensische Hämogenetik e.V.) New Orleans, October 19–21, 1989. 3:98-100

Degree: M.D

المؤلفون: Diéterlen, F., Pinna, A., Berriche, S., Mercier, G., Lucotte, G.

المصدر: International Journal of Anthropology. November 2006 21(2):117-121

المؤلفون: Lucotte, G., Berriche, S., Turpin, J. C.

المصدر: Human Genetics. April 1993 91(3):273-274

المؤلفون: Lucotte, G., Barré, E., Berriche, S.

المصدر: Human Genetics. October 1991 87(6):759-759

المؤلفون: Berriche, S., Turpin, J. C., Lucotte, G.

المصدر: Journal of Neurology. March 1988 235(4):234-235

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المؤلفون: Lucotte, G., François, M.-H., Petit, M.-C., Berriche, S., Réveilleau, S.

المصدر: Molecular and Cellular Probes; October 1993, Vol. 7 Issue: 5 p339-344, 6p

المؤلفون: Lucotte G, Berriche S, J. C. Turpin

المصدر: Journal of neurology. 235(4)

مصطلحات موضوعية: Male, endocrine system, congenital, hereditary, and neonatal diseases and abnormalities, X Chromosome, endocrine system diseases, Biology, Fatty Acids, Nonesterified, medicine, Humans, Allele, Adrenoleukodystrophy, Gene, X chromosome, Alleles, Genetics, Factor VIII, Hybridization probe, Leukodystrophy, nutritional and metabolic diseases, Diffuse Cerebral Sclerosis of Schilder, DNA, medicine.disease, Xq28, Pedigree, Neurology, Genes, Female, Neurology (clinical), Long chain fatty acid, Polymorphism, Restriction Fragment Length

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e503bac95fb919b784ef740a9f0237
https://pubmed.ncbi.nlm.nih.gov/2897431