DNA REPAIR SYNTHESIS IN HUMAN HETEROKARYONS. III. THE RAPID AND SLOW COMPLEMENTING VARIETIES OF XERODERMA PIGMENTOSUMGIANNELLI F; PAWSEY SA.1976; J. CELL RES.; G.B.; DA. 1976; VOL. 20; NO 1; PP. 207-213; BIBL. 8 REF.Article

GENE DOSAGE EFFECT ON HUMAN TRISOMY 16. = EFFET DE DOSE DU GENE DANS LA TRISOMIE 16 HUMAINEMARIMO B; GIANNELLI F.1975; NATURE; G.B.; DA. 1975; VOL. 256; NO 5514; PP. 204-206; BIBL. 18 REF.Article

Factor IXGIANNELLI, F.Baillière's clinical haematology. 1989, Vol 2, Num 4, pp 821-848, issn 0950-3536Article

THE EFFECT OF APHIDICOLIN ON THE RATE OF DNA REPLICATION AND UNSCHEDULED DNA SYNTHESIS OF BLOOM SYNDROME AND NORMAL FIBROBLASTSGIANNELLI F; BOTCHERBY PK; AVERY JA et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 4; PP. 357-359; BIBL. 17 REF.Article

EFFECT OF INCUBATION TEMPERATURE ON THE FREQUENCY OF SISTER CHROMATID EXCHANGES IN BLOOM'S SYNDROME LYMPHOCYTESWEST J; LYTTLETON MJ; GIANNELLI F et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 3; PP. 204-207; BIBL. 31 REF.Article

Direct sequencing of PCR-amplified DNAGREEN, P. M; GIANNELLI, F.Molecular biotechnology. 1994, Vol 1, Num 2, pp 117-124, issn 1073-6085Article

CELLULAR HYPERSENSITIVITY TO UV-A: A CLUE TO THE AETIOLOGY OF ACTINIC RETICULOID.GIANNELLI F; BOTCHERBY PK; MARIMO B et al.1983; LANCET (THE). (BRITISH EDITION); ISSN 0140-6736; GBR; DA. 1983; NO 8316; PP. 88-90; BIBL. 15 REF.Article

ULTRAVIOLET LIGHT SENSITIVITY AND DELAYED DNA-CHAIN MATURATION IN BLOOM'S SYNDROME FIBROBLASTS.GIANNELLI F; BENSON PF; PAWSEY SA et al.1977; NATURE; G.B.; DA. 1977; VOL. 265; NO 5593; PP. 466-469; BIBL. 13 REF.Article

The X chromosome and the rate of deleterious mutations in humansGIANNELLI, F; GREEN, P. M.American journal of human genetics. 2000, Vol 67, Num 2, pp 515-517, issn 0002-9297Article

CLINICAL, GENETIC AND DNA REPAIR STUDIES ON A CONSECUTIVE SERIES OF PATIENTS WITH XERODERMA PIGMENTOSUMPAWSEY SA; MAGNUS IA; RAMSAY CA et al.1979; QUART. J. MED.; GBR; DA. 1979; VOL. 48; NO 190; PP. 179-210; BIBL. 3 P.Article

A HUMAN SUBJECT WITH A NEW DEFECT IN REPAIR OF ULTRAVIOLET DAMAGE.ARLETT CF; LEHMANN AR; GIANNELLI F et al.1978; J. INVEST. DERMATOL.; U.S.A.; DA. 1978; VOL. 70; NO 4; PP. 173-177; BIBL. 42 REF.Article

LO STUDIO DELLA DISTRIBUZIONE VOLUMETRICA NELLE CELLULE EMATICHE QUALE SEMPLICE E RAPIDO SCREENING PER LE BETA ED ALFA-TALASSEMIE = L'ETUDE DE LA DISTRUBTION VOLUMETRIQUE DES CELLULES DU SANG EN TANT QUE DEPISTAGE SIMPLE ET RAPIDE POUR LES BETA ET ALPHA-THALASSEMIESBONANNI G; CIANCARELLI M; FIORITONI G et al.1979; HAEMATOLOGICA; ITA; DA. 1979; VOL. 64; NO 5; PP. 580-585; ABS. ENG; BIBL. 15 REF.Article

The molecular basis of haemophilia A and BGIANNELLI, F; GREEN, P. M.Baillière's clinical haematology. 1996, Vol 9, Num 2, pp 211-228, issn 0950-3536Article

Differences in patterns of complementation of the more common groups of Xeroderma pigmentosum: possible implicationsGIANNELLI, F; PAWSEY, S. A; AVERY, J. A et al.Cell (Cambridge). 1982, Vol 29, Num 2, pp 451-458, issn 0092-8674Article

MODIFICAZIONI ELETTROCARDIOGRAFICHE NELLA IPOTERMIA ACCIDENTALE = MODIFICATIONS ELECTROCARDIOGRAPHIQUES DANS L'HYPOTHERMIE ACCIDENTELLESGOBBA G; NASSISI G; GIANNELLI F et al.1982; G. ITAL. CARDIOL.; ISSN 0390-5403; ITA; DA. 1982; VOL. 12; NO 2; PP. 147-149; ABS. ENG; BIBL. 11 REF.Article

INDUCTION OF GALACTOKINASE IN FIBROBLASTS FROM HETEROZYGOUS AND HOMOZYGOUS SUBJECTSZACCHELLO F; BENSON PF; BROWN S et al.1972; NATURE NEW BIOL.; G.B.; DA. 1972; VOL. 239; NO 90; PP. 95-96; BIBL. 6 REF.Serial Issue

Characterization of the gene (VBP1) and transcript for the von Hippel-Lindau binding protein and isolation of the highly conserved murine homologueBRINKE, A; GREEN, P. M; GIANNELLI, F et al.Genomics (San Diego, Calif.). 1997, Vol 45, Num 1, pp 105-112, issn 0888-7543Article

Mutation rates in humans. I. Overall and sex-specific rates obtained from a population study of hemophilia BGREEN, P. M; SAAD, S; LEWIS, C. M et al.American journal of human genetics. 1999, Vol 65, Num 6, pp 1572-1579, issn 0002-9297Article

Ultrarapid mutation detection by multiplex, solid-phase chemical cleavageROWLEY, G; SAAD, S; GIANNELLI, F et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 3, pp 574-582, issn 0888-7543Article

Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletionLJUNG, R; GREEN, P; SJÖRIN, E et al.European journal of haematology. 1992, Vol 49, Num 4, pp 215-218, issn 0902-4441Article

Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII geneNAYLOR, J. A; GREEN, P. M; MONTANDON, A. J et al.Lancet (British edition). 1991, Vol 337, Num 8742, pp 635-639, issn 0140-6736, 5 p.Article

Haplotype analysis of identical factor IX mutants using PCRGREEN, P. M; MONTANDON, A. J; LJUNG, R et al.Thrombosis and haemostasis. 1992, Vol 67, Num 1, pp 66-69, issn 0340-6245Article

The use of DNA amplification for genetic counselling related diagnosis in haemophilia BTSANG, T. C; BENTLEY, D. R; NILSSON, I. M et al.Thrombosis and haemostasis. 1989, Vol 61, Num 3, pp 343-347, issn 0340-6245Article

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