Cancer in Patients With Ataxia-Telangiectasia and in Their Relatives in the Nordic Countries von Olsen, Jørgen H., Hahnemann, Johanne M., Børresen-Dale, Anne-Lise, Brøndum-Nielsen, Karen, Hammarström, Lennart, Kleinerman, Ruth, Kääriäinen, Helena, Lönnqvist, Tuula, Sankila, Risto, Seersholm, Niels, Tretli, Steinar, Yuen, Jonathan, Boice, John D., Tucker, Margaret

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Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus von MACKAY, D. J. G, HAHNEMANN, J. M. D, CLAYTON-SMITH, J, TEMPLE, I. K, BOONEN, S. E, POERKSEN, S, BUNYAN, D. J, WHITE, H. E, DURSTON, V. J, THOMAS, N. S, ROBINSON, D. O, SHIELD, J. P. H

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A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus von MACKAY, D. J. G, BOONEN, S. E, SHIELD, J. P. H, WHITE, H. E, TEMPLE, I. K, CLAYTON-SMITH, J, GOODSHIP, J, HAHNEMANN, J. M. D, KANT, S. G, NJOLSTAD, P. R, ROBIN, N. H, ROBINSON, D. O, SIEBERT, R

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Accuracy of cytogenetic findings on Chorionic Villus Sampling (CVS)-diagnostic consequences of CVS Mosaicism and non-Mosaic Discrepancy in Centres contributing to EUCROMIC 1986-199... von Hahnemann, Johanne M., Vejerslev, Lars O.

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A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus von Mackay, D J G, Boonen, S E, Clayton-Smith, J, Goodship, J, Hahnemann, J M D, Kant, S G, Njølstad, P R, Robin, N H, Robinson, D O, Siebert, R, Shield, J P H, White, H E, Temple, I K

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Characterization of ATM mutations in 41 Nordic families with Ataxia Telangiectasia von Laake, K., Jansen, L., Hahnemann, J.M., Brøndum-Nielsen, K., Lönnqvist, T., Kääriäinen, H., Sankila, R., Lähdesmäki, A., Hammarström, L., Yuen, J., Tretli, S., Heiberg, A., Olsen, J.H., Tucker, M., Kleinerman, R., Børresen-Dale, A-L.

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Breast and other cancers in 1445 blood relatives of 75 Nordic patients with ataxia telangiectasia von OLSEN, J. H, HAHNEMANN, J. M. D, BRØNDUM-NIELSEN, K, YUEN, J, TUCKER, M, BØRRESEN-DALE, A.-L, TRETLI, S, KLEINERMAN, R, SANKILA, R, HAMMARSTRÖM, L, ROBSAHM, T. E, KÄÄRIÄINEN, H, BREGARD, A

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Late relapse of adrenocortical carcinoma in Beckwith-Wiedemann syndrome. Clinical, endocrinological and genetic aspects von Hertel, NT, Carlsen, N, Kerndrup, G, Pedersen, IL, Clausen, N, Hahnemann, JMD, Jacobsen, BB

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Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver–Russell syndrome and growth retardation von Grønskov, Karen, Poole, Rebecca L, Hahnemann, Johanne M D, Thomson, Jennifer, Tümer, Zeynep, Brøndum-Nielsen, Karen, Murphy, Rinki, Ravn, Kirstine, Melchior, Linea, Dedic, Alma, Dolmer, Birgitte, Temple, I Karen, Boonen, Susanne E, Mackay, Deborah J G

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Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD von European Collaborative Research on Mosaicism in CVS (EUCROMIC)

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European collaborative research on mosaicism in CVS (EUCROMIC)-fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomy von Hahnemann, Johanne M., Vejerslev, Lars O.

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Prenatal and postnatal prevalence of Turner's syndrome. No reason to doubt standard of prenatal diagnosis von Hahnemann, J M, Vejerslev, L O

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Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism von Karadima, G, Bugge, M, Nicolaidis, P, Vassilopoulos, D, Avramopoulos, D, Grigoriadou, M, Albrecht, B, Passarge, E, Annerén, G, Blennow, E, Clausen, N, Galla-Voumvouraki, A, Tsezou, A, Kitsiou-Tzeli, S, Hahnemann, J M, Hertz, J M, Houge, G, Kuklík, M, Macek, M, Lacombe, D, Miller, K, Moncla, A, López Pajares, I, Patsalis, P C, Petersen, M B

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Reply: Increased risk of breast cancer among female relatives of patients with Ataxia-Telangiectasia: a causal relationship? von Olsen, J H, Hahnemann, J M D, Børresen-Dale, A-L, Tretli, S, Kleinerman, R, Sankila, R, Hammarström, L, Robsahm, T E, Kääriäinen, H, Bregård, A, Brøndum-Nielsen, K, Yuen, J, Tucker, M

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Absence of nasal bone and detection of trisomy 21 von Hutchon, David JR

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Absence of nasal bone and detection of trisomy 21 von Hjalgrim, Helle, Hahnemann, Johanne M, Kjaer, Inger, Broendum-Nielsen, Karen

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No reason to doubt standard of prenatal diagnosis von Hahnemann, Johanne M, Vejerslev, Lars O

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Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia von Laake, K, Jansen, L, Hahnemann, JM, Brondum-Nielsen, K, Lonnqvist, T, Kaariainen, H, Sankila, R, Lahdesmaki, A, Hammarstrom, L, Yuen, J, Tretli, S, Heiberg, A, Olsen, JH, Tucker, M, Kleinerman, R, Borresen-Dale, AL

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Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism von Karadima, G, Bugge, M, Nicolaidis, P, Vassilopoulos, D, von Beust, G, Pajares, IL, Albrecht, B, Anneren, G, Avramopoulos, D, Blennow, E, Brondum-Nielsen, K, Clausen, N, Galla-Voumvouraki, A, Grigoriadou, M, Hahnemann, JM, Hertz, JM, Kitsiou-Tzeli, S, Lacombe, D, Miller, K, Moncla, A, Passarge, E, Patsalis, PC, Prieur, M, Tsezou, A, Vekemans, M, Petersen, MB

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Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57 von Mackay, Deborah J G, Callaway, Jonathan L A, Marks, Sophie M, White, Helen E, Acerini, Carlo L, Boonen, Susanne E, Dayanikli, Pinar, Firth, Helen V, Goodship, Judith A, Haemers, Andreas P, Hahnemann, Johanne M D, Kordonouri, Olga, Masoud, Ahmed F, Oestergaard, Elsebet, Storr, John, Ellard, Sian, Hattersley, Andrew T, Robinson, David O, Temple, I Karen

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