A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnosesBOUE, A; GALLANO, P.Prenatal diagnosis. 1984, Vol 4, pp 45-67, issn 0197-3851Article

Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of the European collaborative prenatal diagnosis centresDANIEL, A; BOUE, A; GALLANO, P et al.Prenatal diagnosis. 1986, Vol 6, Num 5, pp 315-350, issn 0197-3851Article

A novel insertional mutation of a single base in exon 12 of the dystrophin geneLASA, A; GALLANO, P; COLOMER, J et al.Clinical genetics. 1995, Vol 48, Num 3, pp 128-130, issn 0009-9163Article

DMD carrier detection in a female with mosaic Turner's syndromeBAIGET, M; TIZZANO, E; VOLPINI, V et al.Journal of medical genetics. 1991, Vol 28, Num 3, pp 209-210, issn 0022-2593Article

High prevalence of the β-thalassaemia nonsense 37 mutation in catalonians from the ebro deltaGALLANO, P; GIRODON, E; GHALEM, N et al.British journal of haematology. 1992, Vol 81, Num 1, pp 126-127, issn 0007-1048Article

Detection of a rare allele with the pMP6d-9/MspI RFLP near the cystic fibrosis locusNUNES, V; CASALS, T; GALLANO, P et al.Human genetics. 1989, Vol 83, Num 3, pp 305-306, issn 0340-6717, 2 p.Article

Symptomatic dysferlin gene mutation carriers : Characterization of two casesILLA, I; DE LUNA, N; DOMINGUEZ-PERLES, R et al.Neurology. 2007, Vol 68, Num 16, pp 1284-1289, issn 0028-3878, 6 p.Article

Calpainopathy : A survey of mutations and polymorphismsRICHARD, I; ROUDAUT, C; GALLANO, P et al.American journal of human genetics. 1999, Vol 64, Num 6, pp 1524-1540, issn 0002-9297Article

Isolated cardiomyopathy caused by a DMD nonsense mutation in somatic mosaicism: genetic normalization in skeletal muscleJUAN-MATEU, J; PARADAS, C; OLIVE, M et al.Clinical genetics. 2012, Vol 82, Num 6, pp 574-578, issn 0009-9163, 5 p.Article

The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specificJEANPIERRE, M; WEIL, D; GALLANO, P et al.Human genetics. 1985, Vol 70, Num 4, pp 302-310, issn 0340-6717Article

Homogeneous phenotype of the gypsy limb-girdle MD with the γ-sarcoglycan C283Y mutationMERLINI, L; KAPLAN, J.-C; KALAYDJIEVA, L et al.Neurology. 2000, Vol 54, Num 5, pp 1075-1079, issn 0028-3878Article

Diagnostic moléculaire des myopathies de Duchenne et de Becker: données actuelles = Molecular diagnosis of Duchenne and Becker muscular dystrophyJUNIEN, C; BOUE, J; DUROS, C et al.Annales de génétique (Paris). 1987, Vol 30, Num 1, pp 5-16, issn 0003-3995Article

The proα2(V) collagen gene (COL5A2) maps to 2q14→2q32, syntenic to the proα1(III) collagen locus (COL3A1)HUERRE-JEANPIERRE, C; HENRY, I; BERNARD, M et al.Human genetics. 1986, Vol 73, Num 1, pp 64-67, issn 0340-6717Article

The structural gene for aldolase B(ALDB) maps to 9qk3→32HENRY, I; GALLANO, P; BESMOND, C et al.Annals of human genetics. 1985, Vol 49, Num 3, pp 173-180, issn 0003-4800Article

Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish familiesDE DIEGO, C; GAMEZ, J; PLASSART-SCHIESS, E et al.Journal of neurology. 1999, Vol 246, Num 9, pp 825-829, issn 0340-5354Article

Severe mental retardation in a young boy with an in-frame deletion in the dystrophin geneCOLOMER, J; GALLANO, P; NICHOLSON, L. V. B et al.European journal of pediatrics. 1994, Vol 153, Num 7, pp 492-494, issn 0340-6199Article

Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRPESTIVILL, X; MCLEAN, C; NUNES, V et al.American journal of human genetics. 1989, Vol 44, Num 5, pp 704-710, issn 0002-9297Article

Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two South European populationsESTIVILL, X; GASPARINI, P; NOVELLI, G et al.Human genetics. 1989, Vol 83, Num 2, pp 175-178, issn 0340-6717Article

Diagnostic moléculaire des myopathies de Duchenne et de Becker. Données actuelles = Molecular diagnosis of Duchenne and Becker muscular dystrophyJUNIEN, C; BOUE, J; DUROS, C et al.La Semaine des hôpitaux de Paris. 1988, Vol 64, Num 4, pp 241-252, issn 0037-1777Article

Segregation analysis of balanced pericentric inversions in pedigree dataSHERMAN, S. L; ISELIUS, L; NORDENSSON, I et al.Clinical genetics. 1986, Vol 30, Num 2, pp 87-94, issn 0009-9163Article