POSTERIOR BUTTOCK PAIN FOLLOWING TOTAL HIP REPLACEMENT = DOULEUR POSTERIEURE DE LA FESSE APRES REMPLACEMENT TOTAL DE LA HANCHEMALLORY TH; HALLEY D.1973; CLIN. ORTHOP. RELAT. RES.; U.S.A.; DA. 1973; NO 90; PP. 104-106; BIBL. 4REF.Serial Issue

RAPID PRENATAL DIAGNOSIS OF THE LESCH-NYHAN SYNDROME.HALLEY D; HEUKELS DULLY MJ.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 2; PP. 100-102; BIBL. 6 REF.Article

Temperature and magnetic field dependence of the Carrier mobility in SOI-wafers by the pseudo-MOSFET methodROSSEL, C; HALLEY, D; CRISTOLOVEANU, S et al.Proceedings - Electrochemical Society. 2003, pp 479-486, issn 0161-6374, isbn 1-56677-375-X, 8 p.Conference Paper

COMPARISON OF THE RESIDUAL ACIDIO ALPHA -D-MANNOSIDASE IN THREE CASES OF MANNOSIDOSISBURDITT L; CHOTAI K; HALLEY D et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 104; NO 2; PP. 201-209; BIBL. 24 REF.Article

IN VITRO STUDIES ON THE INTERCELLULAR EXCHANGE OF LYSOSOMAL ENZYMES BETWEEN NORMAL AND ENZYME DEFICIENT HUMAN FIBROBLASTS. = ETUDES IN VITRO SUR L'ECHANGE INTERCELLULAIRE DES ENZYMES LYSOSOMIQUES ENTRE FIBROBLASTES HUMAINS NORMAUX ET CARENCES EN ENZYMEREUSER AJJ; MULDER MP; HALLEY D et al.1975; HISTOCHEM. J.; G.B.; DA. 1975; VOL. 7; NO 6; PP. 502-504; BIBL. 4 REF.Article

Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co-segregates with tuberous sclerosis complex in mildly affected kindredsWENTINK, M; NELLIST, M; SMEETS, E et al.Clinical genetics. 2012, Vol 81, Num 5, pp 453-461, issn 0009-9163, 9 p.Article

MBE-grown epitaxial oxides for advanced gate stackFOMPEYRINE, J; NORGA, G; GUILLER, A et al.WODIM : workshop on dielectrics in microelectronics. 2003, pp 65-68, isbn 2-9514840-0-3, 4 p.Conference Paper

Linkage analysis under locus heterogeneity : Behaviour of the A-test in complex analysesJANSSEN, B; HALLEY, D; SANDKUIJL, L et al.Human heredity. 1997, Vol 47, Num 4, pp 223-233, issn 0001-5652Article

Alliages magnétiques FePd et FePt en couches minces sous contrainte épitaxiale : mise en ordre en température et propriétés magnétiques = Thin layers of FePd and FePt magnetic alloys with epitaxial constraint : ordering by thermal treatment and magnetic propertiesARENAL DE LA CONCHA, R; SCHUSTER, I; HALLEY, D et al.Journal de physique. IV. 2002, Vol 97, pp pr6.25-pr6.38, issn 1155-4339Conference Paper

Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13TAKAHASHI, M; RAPLEY, E; EVANS, D. G et al.Human genetics. 2000, Vol 106, Num 1, pp 58-65, issn 0340-6717Article

Interaction between hamartin and tuberin, the TSC1 and TSC2 gene productsVAN SLEGTENHORST, M; NELLIST, M; NAGELKERKEN, B et al.Human molecular genetics (Print). 1998, Vol 7, Num 6, pp 1053-1057, issn 0964-6906Article

Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1HUMPHREY, D; KWIATKOWSKA, J; HENSKE, E. P et al.Annals of human genetics. 1997, Vol 61, pp 299-305, issn 0003-4800, 4Article

Linkage relationships and allelic associations of the cystic fibrosis locus and four marker lociSCHMIDTKE, J; KRAWCZAK, M; FREY, D et al.Human genetics. 1987, Vol 76, Num 4, pp 337-343, issn 0340-6717Conference Paper

Cognitive impairment in tuberous sclerosis complex is a multifactorial conditionJANSEN, F. E; VINCKEN, K. L; VAN HUFFELEN, A. C et al.Neurology. 2008, Vol 70, Num 12, pp 916-923, issn 0028-3878, 8 p.Article

X-ray absorption near-edge structure and valence state of Mn in (Ga,Mn)NTITOV, A; BIQUARD, X; KULATOV, E et al.Physical review B. Condensed matter and materials physics. 2005, Vol 72, Num 11, pp 115209.1-115209.7, issn 1098-0121Article

Magnetic properties of irradiated highly anisotropic materialsRAVELOSONA, D; DEVOLDER, T; BERNAS, H et al.IEEE transactions on magnetics. 2001, Vol 37, Num 4, pp 1643-1645, issn 0018-9464, 1Conference Paper

A 1.7-Megabase sequence-ready cosmid contig covering the TSC1 candidate region in 9q34HORNIGOLD, N; VAN SLEGTENHORST, M; NAHMIAS, J et al.Genomics (San Diego, Calif.). 1997, Vol 41, Num 3, pp 385-389, issn 0888-7543Article

Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8DEAN, M; AMOS, J. A; WEIR, B. S et al.Human genetics. 1990, Vol 85, Num 3, pp 275-278, issn 0340-6717, 4 p.Article

Prenatal diagnosis of cystic fibrosis using linked DNA probesSCHWARTZ, M; SUPER, M; SCHMIDTKE, J et al.Prenatal diagnosis. 1988, Vol 8, Num 8, pp 619-624, issn 0197-3851Article

Seven cases of Pompe disease from GreeceKROOS, M; MANTA, P; MAVRIDOU, I et al.Journal of inherited metabolic disease. 2006, Vol 29, Num 4, pp 556-563, issn 0141-8955, 8 p.Article

Pre-edge features in X-ray absorption structure of Mn in GaMnN, GaMnAs and GeMnTITOV, A; KULATOV, E; USPENSKII, Yu. A et al.Journal of magnetism and magnetic materials. 2006, Vol 300, Num 1, pp 144-147, issn 0304-8853, 4 p.Conference Paper

The TSC1 gene product, hamartin, negatively regulates cell proliferationMILOLOZA, A; ROSNER, M; NELLIST, M et al.Human molecular genetics (Print). 2000, Vol 9, Num 12, pp 1721-1727, issn 0964-6906Article

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer familiesPEELEN, T; VAN VLIET, M; VAN DER LUIJT, R et al.American journal of human genetics. 1997, Vol 60, Num 5, pp 1041-1049, issn 0002-9297Article

Refined localization of TSC1 by combined analysis of 9q34 and 16p13 data in 14 tuberous sclerosis familiesJANSSEN, B; SAMPSON, J; SANDKUIJL, L et al.Human genetics. 1994, Vol 94, Num 4, pp 437-440, issn 0340-6717Article

Different haplotypes for cystic fibrosis-linked DNA polymorphisms in Polish and Dutch populationsMACIEJKO, D; BAL, J; MAZURCZAK, T et al.Human genetics. 1989, Vol 83, Num 3, pp 220-222, issn 0340-6717, 3 p.Article