Genetic determination of exocrine pancreatic function in cysti fibrosisKRISTIDIS, P; BOZON, D; COREY, M et al.American journal of human genetics. 1992, Vol 50, Num 6, pp 1178-1184, issn 0002-9297Article

Demonstration of an apple-core lesion by small bowel enteroclysis : an atypical detection of gallbladder carcinomaBOUTEMY, R; VOLLONT, G. H; TACK, D et al.Journal belge de radiologie (1907). 1994, Vol 77, Num 6, pp 280-281, issn 0021-7646Article

The relation between genotype and phenotype in cystic fibrosis : analysis of the most common mutation (ΔF₅₀₈)KEREM, E; COREY, M; BAT-SHEVA KEREM et al.The New England journal of medicine. 1990, Vol 323, Num 22, pp 1517-1522, issn 0028-4793Article

Chemical synthesis of a biologically active gene for human immune interferon-γ: prospect for site-specific mutagenesis and structure-function studiesJAY, E; MACKNIGHT, D; PAWLAK, J et al.The Journal of biological chemistry (Print). 1984, Vol 259, Num 10, pp 6311-6317, issn 0021-9258Article

Hemorrhage in the cavum septi pellucidi in a full-term neonateBOUTEMY, R; DAN, B; CHRISTOPHE, C et al.Pediatric radiology. 1997, Vol 27, Num 2, pp 144-146, issn 0301-0449Article

The complete BRCA2 gene and mutations in chromosome 13q-linked kindredsTAVTIGIAN, S. V; SIMARD, J; BELANGER, C et al.Nature genetics. 1996, Vol 12, Num 3, pp 333-337, issn 1061-4036Article

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsOSBORNE, L. R; MARTINDALE, D; ROMMENS, J et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 2, pp 328-336, issn 0888-7543Article

A new class of electron transport compounds: 1,3-bis-dicyanomethylene indanesROMMENS, J; VAN DER AUWERAER, M; DE SCGRYVER, F. C et al.Advanced materials (Weinheim). 1995, Vol 7, Num 6, pp 574-576, issn 0935-9648Article

Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35VAN DEUTEKOM, J. C. T; HOFKER, M. H; ROMBERG, S et al.Muscle & nerve. 1995, pp S19-S26, issn 0148-639X, SUP2Conference Paper

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephalyWALLIS, D. E; ROESSLER, E; HEHR, U et al.Nature genetics. 1999, Vol 22, Num 2, pp 196-198, issn 1061-4036Article

BRCA2 germline mutations in male breast cancer cases and breast cancer familiesCOUCH, F. J; FARID, L. M; SHATTUCK-EIDENS, D et al.Nature genetics. 1996, Vol 13, Num 1, pp 123-125, issn 1061-4036Article

Giant colonic diverticulum : presentation of one case and review of the literatureROGER, T; ROMMENS, J; BAILLY, J.-M et al.Abdominal imaging. 1996, Vol 21, Num 6, pp 530-533, issn 0942-8925Article

Intramural esophageal cyst: the role of endoscopic ultrasonographyROMMENS, J; DEVIERE, J; GEVENOIS, P. A et al.Journal belge de radiologie (1907). 1994, Vol 77, Num 1, pp 15-16, issn 0021-7646Article

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer familiesSIMARD, J; TONIN, P; LIU, Q et al.Nature genetics. 1994, Vol 8, Num 4, pp 392-398, issn 1061-4036Article

High-level expression of a chemically synthetized gene for human interferon-γ using a prokaryotic expression vectorJAY, E; ROMMENS, J; JAY, F et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1984, Vol 81, Num 8, pp 2290-2294, issn 0273-1134Article

Gene expression: chemical synthesis and molecular cloning of a bacteriophage T₅(T5P25) early promoterROMMENS, J; MACKNIGHT, D; POMEROY-CLONEY, L et al.Nucleic acids research. 1983, Vol 11, Num 17, pp 5921-5940, issn 0305-1048Article

Explorations radiologiques de l'impuissance = Radiology of impotenceDELCOUR, C;; BRUNINX, G;; ROGER, T; et al.Revue d'imagerie médicale. 1994, Vol 6, Num 6, pp 335-344, issn 0998-4321Article

Identification of sequences of chromosome 7 that are expressed in sweat gland epithelial cellsBURNS, J; MELMER, G; ROMMENS, J. M et al.Human genetics. 1990, Vol 85, Num 2, pp 151-156, issn 0340-6717Article

Dinucleotide repeat polymorphism near the RP3 locus in Xp21 (DXS1110)ROUX, A.-F; CHU CHIN YUAN; ROMMENS, J. M et al.Human molecular genetics (Print). 1993, Vol 2, Num 6, issn 0964-6906, p. 821Article

Right-angle light scattering to assay basal and regulated plasma membrane Cl^- conductancesDHO, S; CHOU, S; XIU-BAO CHANG et al.American journal of physiology. Cell physiology. 1992, Vol 32, Num 2, pp C530-C534, issn 0363-6143Article

Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDSMÄKLTIE, O; ELLIS, L; DURIE, P. R et al.Clinical genetics. 2004, Vol 65, Num 2, pp 101-112, issn 0009-9163, 12 p.Article

Segregation analysis in Shwachman-Diamond syndrome : Evidence for recessive inheritanceGINZBERG, H; SHIN, J; ELLIS, L et al.American journal of human genetics. 2000, Vol 66, Num 4, pp 1413-1416, issn 0002-9297Article

Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621+1G→T and 711+1G→T mutationsZIELENSKI, J; BOZON, D; MARKIEWICZ, D et al.Human molecular genetics (Print). 1993, Vol 2, Num 6, pp 683-687, issn 0964-6906Article

Physical localization of two DNA markers closely linked to the cystic fibrosis locus by pulsed-field gel electrophoresisROMMENS, J. M; ZENGERLING-LENTES, S; BAT-SHEVA KEREM et al.American journal of human genetics. 1989, Vol 45, Num 6, pp 932-941, issn 0002-9297Article

Sequence of the murine Huntington disease gene: evidence for conservatioin, and polymorphism in a triplet (CCG) repeat alternate splicingBIAOYANG LIN; JAMAL NASIR; MACDONALD, H et al.Human molecular genetics (Print). 1994, Vol 3, Num 1, pp 85-92, issn 0964-6906Article