Localization of the gene for Cowden disease to chromosome 10q22-23
Nelen, M.R, Padberg, G.W, Peeters, E.A.J, Lin, A.Y, Helm, B. van den, Frants, R.R, Goulon, V, Goldstein, A.M, Reen, M.M.M van, Eastern, D.F, Eeles, R.A, Hodgson, S, Mulvihill, J.J, Murday, V.A, Tucker, M.A, Mariman, E.C.M, Starink, T.M, Ponder, B.A.J, Ropers, H.H, Kremer, H, Longy, M, Eng, C
Published in Nature genetics (01.05.1996)
Published in Nature genetics (01.05.1996)
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An exact general analysis of ligand binding displacement and saturation curves
van Zoelen, E. J. J, Kramer, R. H, van Reen, M. M. M, Veerkamp, J. H, Ross, H. A
Published in Biochemistry (Easton) (22.06.1993)
Published in Biochemistry (Easton) (22.06.1993)
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A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male lh-independent precocious puberty
KREMERT, H, MARTENS, J. W. M, POTAU, N, BUCKLER, J. M. H, JANSEN, M, PARKS, J. S, LATIF, H. A, MOLL, G. W, EPPING, W, SAGGESE, G, MARIMAN, E. C. M, THEMMEN, A. P. N, VAN REEN, M, BRUNNER, H. G, VERHOEF-POST, M, WIT, J. M, OTTEN, B. J, DROP, S. L. S, DE WAAL, H. A. D.-V, POMBO-ARIAS, M, DE LUCA, F
Published in The journal of clinical endocrinology and metabolism (01.03.1999)
Published in The journal of clinical endocrinology and metabolism (01.03.1999)
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Mutation analysis in the candidate Möbius syndrome genes PGT and GATA2 on chromosome 3 and EGR2 on chromosome 10
van der Zwaag, B, Verzijl, H T F M, Beltran-Valero de Bernabe, D, Schuster, V L, van Bokhoven, H, Kremer, H, van Reen, M, Wichers, G H, Brunner, H G, Padberg, G W
Published in Journal of medical genetics (01.06.2002)
Published in Journal of medical genetics (01.06.2002)
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A Limited Repertoire of Mutations of the Luteinizing Hormone (LH) Receptor Gene in Familial and Sporadic Patients with Male LH-Independent Precocious Puberty1
Kremer, H, Martens, J. W. M, van Reen, M, Verhoef-Post, M, Wit, J. M, Otten, B. J, Drop, S. L. S, Delemarre-van de Waal, H. A, Pombo-Arias, M, De Luca, F, Potau, N, Buckler, J. M. H, Jansen, M, Parks, J. S, Latif, H. A, Moll, G. W, Epping, W, Saggese, G, Mariman, E. C. M, Themmen, A. P. N, Brunner, H. G
Published in The journal of clinical endocrinology and metabolism (01.03.1999)
Published in The journal of clinical endocrinology and metabolism (01.03.1999)
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Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene
Milgrom, Edwin, Ropers, Hans-Hilger, Themmen, Axel P.N, Brunner, Han G, Toledo, Sergio P.A, Fridman, Julia B, Hayashida, Cesar Y, Mariman, Edwin, Kraaij, Robert, Post, Miriam, Kremer, Hannie, Reen, Margo van
Published in Nature genetics (01.02.1995)
Published in Nature genetics (01.02.1995)
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Mapping a gene for Noonan syndrome to the long arm of chromosome 12
Patton, Michael A, van der Burgt, Ineke, van Reen, Margo, Hol, Frans, Mariman, Edwin, Elsawi, Madiha M, Jamieson, C. Ruth, Brady, Angela F, Jeffery, Steve
Published in Nature genetics (01.12.1994)
Published in Nature genetics (01.12.1994)
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Localization of a Gene for Möbius Syndrome to Chromosome 3q by Linkage Analysis in a Dutch Family
Kremer, Hannie, Kuyt, Lambertus P., van den Helm, Bellinda, van Reen, Margo, Leunissen, Jack A. M., Hamel, Ben C. J., Jansen, Cees, Mariman, Edwin C. M., Frants, Rune R., Padberg, George W.
Published in Human molecular genetics (01.09.1996)
Published in Human molecular genetics (01.09.1996)
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Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6
Ion, A, Crosby, A H, Kremer, H, Kenmochi, N, Van Reen, M, Fenske, C, Van Der Burgt, I, Brunner, H G, Montgomery, K, Kucherlapati, R S, Patton, M A, Page, C, Mariman, E, Jeffery, S
Published in Journal of medical genetics (01.11.2000)
Published in Journal of medical genetics (01.11.2000)
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Journal Article
Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2,DCN, EPS8, andRPL6
ION, A, CROSBY, A H, KREMER, H, KENMOCHI, N, VAN REEN, M, FENSKE, C, VAN DER BURGT, I, BRUNNER, H G, MONTGOMERY, K, KUCHERLAPATI, R S, PATTON, M A, PAGE, D C, MARIMAN, E, JEFFERY, S
Published in Journal of medical genetics (01.11.2000)
Published in Journal of medical genetics (01.11.2000)
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Further Delineation of the Critical Region for Noonan Syndrome on the Long Arm of Chromosome 12
Brady, Angela F., Jamieson, C. Ruth, van der Burgt, Ineke, Crosby, Andrew, van Reen, Margo, Kremer, Hannie, Mariman, Edwin, Patton, Michael A., Jeffery, Steve
Published in European journal of human genetics : EJHG (01.09.1997)
Published in European journal of human genetics : EJHG (01.09.1997)
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Localization of a gene for Moebius syndrome to chromosome 3q by linkage analysis in a Dutch family
Kremer, H, Kuyt, L P, van den Helm, B, van Reen, M, Leunissen, JAM, Hamel, BCJ, Jansen, C, Mariman, ECM, Frants, R R, Padberg, G W
Published in Human molecular genetics (01.01.1996)
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Published in Human molecular genetics (01.01.1996)
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