Human Genetics
Collection
Collection
- ISSN: 03406717
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Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter Article
Human Genetics, 84(3), 219-222.J.P. Dumanski (Jan), A.H.M. Geurts van Kessel (Ad), M. Ruttledge (Martin), A. Wladis (Andreas), N. Sugawa (Noriaki), V.P. Collins (Peter) and M. Nordenskjöld
February 1990
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Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8 Article
Human Genetics, 85(3), 275-278.M. Dean (Michael Emmans), W. Amos, J. Lynch, G. Romeo (Giovanni), M. Devoto (Marcella), K. Ward (Ken), D.J.J. Halley (Dicky), B.A. Oostra (Ben), M. Ferrari (Maurizio), S. Russo (Sascha), et al. B.S. Weir (Bruce), P.B. Finn (Paula), F.S. Collins (Francis) and M.C. Iannuzzi (Michael)
August 1990
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Distribution and characterization of a Sandhoff disease-associated 50-kb deletion in the gene encoding the human β-hexosaminidase β-chain Article
Human Genetics, 85(3), 327-329.H. Bikker (Hennie), F.M. van den Berg (Frank), R.A. Wolterman (Ruud), W.J. Kleijer (Wim), J.J.M. de Vijlder (Jan) and P.A. Bolhuis (P.)
August 1990
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Localization of the cellular retinoic acid binding protein (CRABP) gene relative to the acute promyelocytic leukemia-associated breakpoint on human chromosome 15 Article
Human Genetics, 87(2), 201-204.A.H.M. Geurts van Kessel (Ad), H. de Leeuw (H.), E.J. Dekker (Erik Jan), J.M. Rijks (Jolianne), N. Spurr (N.), A.M. Ledbetter (Andrew M.), E. Kootwijk (E.) and M.J. Vaessen (Marie-Josée)
June 1991
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New distal marker closely linked to the fragile X locus Article
Human Genetics, 87(3), 369-372.T. Hulsebos (Theo), B.A. Oostra (Ben), A. Broersen (Alexander), A. Smits, B.A. van Oost (B.) and A. Westerveld (Andries)
July 1991
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Ataxia-telangiectasia: Linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome Article
Human Genetics, 88(6), 619-626.Y. Ziv (Yael), M. Frydman (Moshe), E.M. Lange (Ethan), N. Zelnik (N.), G. Rotman (Galit), C. Julier (C.), N.G.J. Jaspers (Nicolaas), E. Dagan (Efrat), D. Abeliovicz (Dvorah), H. Dar (H.), et al. Z. Borochowitz (Z.), M. Lathrop (Mark), A. Gatti (Arianna) and Y. Shiloh (Yosef)
March 1992
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Characterization of a new mutation (R292G) and a deletion at the human uroporphyrinogen decarboxylase locus in two patients with hepatoerythropoietic porphyria Article
Human Genetics, 89(5), 548-552.H. de Verneuil1 (Hubert), F. Bourgeois (Francine), F.W.M. de Rooij (Felix), P.D. Siersema (Peter), J.H.P. Wilson (Paul), B. Grandchamp (Bernard) and Y. Nordmann (Yves)
July 1992
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Etiological aspects of congenital diaphragmatic hernia: results of a case comparison study Article
Human Genetics, 94(4), 445-446.A.P. Bos (Albert), A.M. Pattenier (Annemieke), D.E. Grobbee (Diederick), D. Lindhout (Dick), D. Tibboel (Dick) and J.C. Molenaar
October 1994