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Maximilian Muenke

Veröffentlichungen von Maximilian Muenke zu Muenke, Maximilian ->
weitere Veröffentlichungen von Maximilian Muenke:
The pit, the cleft and the web (2002)
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly (1996)
Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes (1996)
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome (1994)
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired (1998)
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly (1999)
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination (2000)
Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes (1993)
Physical mapping of the holoprosencephaly critical region on chromosome 7q36 (1993)
Loss-of-function mutations in the EGF-CFC gene CFC1 are associatedwith human left-right laterality defects (2000)
Cbfβ interacts with Runx2 and has a critical role in bone development (2002)
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2 (1995)
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22 (1997)
Familial dementia caused by polymerization of mutant neuroserpin (1999)
Veröffentlichungen zu Muenke, Maximilian
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1
Muenke, Maximilian The pit, the cleft and the web
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 32, No. 2 (2002), p. 219-220
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2002
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2
Roessler, Erich, Belloni, Elena, ... Mutations in the human Sonic Hedgehog gene cause holoprosencephaly
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 14, No. 3 (1996), p. 357-360
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1996
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3
Bellus, Gary A., Gaudenz, Karin, ... Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 14, No. 2 (1996), p. 174-176
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1996
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4
Muenke, Maximilian, Schell, Ute, ... A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 8, No. 3 (1994), p. 269-274
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1994
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5
Brown, Stephen A., Warburton, Dorothy, ... Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 20, No. 2 (1998), p. 180-183
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1998
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6
Wallis, Deeann E., Roessler, Erich, ... Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 22, No. 2 (1999), p. 196-198
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1999
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7
Gripp, Karen W., Wotton, David, ... Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 25, No. 2 (2000), p. 205-208
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2000
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8
Tyler-Smith, Chris, Oakey, Rebecca J., ... Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 5, No. 4 (1993), p. 368-375
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1993
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9
Gurrieri, Fiorella, Trask, Barbara J., ... Physical mapping of the holoprosencephaly critical region on chromosome 7q36
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 3, No. 3 (1993), p. 247-251
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1993
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10
Bamford, Richard N., Roessler, Erich, ... Loss-of-function mutations in the EGF-CFC gene CFC1 are associatedwith human left-right laterality defects
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 26, No. 3 (2000), p. 365-369
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2000
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11
Kundu, Mondira, Javed, Amjad, ... Cbfβ interacts with Runx2 and has a critical role in bone development
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 32, No. 4 (2002), p. 639-644
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2002
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12
Robin, Nathaniel H., Feldman, George J., ... Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 11, No. 4 (1995), p. 459-461
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1995
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13
Quaderi, Nandita A., Schweiger, Susann, ... Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 17, No. 3 (1997), p. 285-291
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1997
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14
Davis, Richard L., Shrimpton, Antony E., ... Familial dementia caused by polymerization of mutant neuroserpin
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 401, No. 6751 (1999), p. 376-379
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1999