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Muenke Maximilian
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http://hub.abes.fr/bmj/periodical/jmg/2009/volume_47/issue_8/B35958AFAF7D6AAFE053120B220A26C8/authorship/41
http://hub.abes.fr/bmj/periodical/archdischild/2002/volume_86/issue_4/B35305B437840CF1E053120B220A6A4C/authorship/4
http://hub.abes.fr/bmj/periodical/jmedgenet/2006/volume_43/issue_2/B3598D6B63057CBEE053120B220A90C5/authorship/7
http://hub.abes.fr/oup/periodical/jpepsy/2008/volume_33/issue_10/101093jpepsyjsn049/authorship/3
http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_24/101093hmgddn294/authorship/9
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_suppl1/101093hmgddg058/authorship/2
http://hub.abes.fr/bmj/periodical/jmedgenet/2006/volume_43/issue_6/B3598D6B63587CBEE053120B220A90C5/authorship/15
http://hub.abes.fr/bmj/periodical/jmedgenet/2007/volume_44/issue_5/B3598D6B63FF7CBEE053120B220A90C5/authorship/11
http://hub.abes.fr/oup/periodical/hmg/2005/volume_14/issue_15/101093hmgddi222/authorship/7
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_13/101093hmg8132479/authorship/17
http://hub.abes.fr/oup/periodical/jpepsy/2006/volume_31/issue_9/101093jpepsyjsj106/authorship/8
http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_12/101093hmg3122153/authorship/17
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_1/101093hmg61137/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_8/101093hmg108791/authorship/13
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_11/101093hmg6111847/authorship/7
http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_3/101093hmg43323/authorship/13
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_11/101093hmg6111937/authorship/16
http://hub.abes.fr/oup/periodical/hmg/1996/volume_5/issue_2/101093hmg52223/authorship/16
http://hub.abes.fr/bmj/periodical/jmedgenet/2005/volume_42/issue_2/B3598D6B623C7CBEE053120B220A90C5/authorship/7
http://hub.abes.fr/bmj/periodical/jmg/2009/volume_46/issue_6/B3598D6B65357CBEE053120B220A90C5/authorship/46
http://hub.abes.fr/bmj/periodical/jmg/2012/volume_49/issue_7/B35958AFB08E6AAFE053120B220A26C8/authorship/45
http://hub.abes.fr/springer/periodical/223/1996/volume_59/issue_2/B934FD18FADC29C2E053120B220AF090/authorship/4
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Abstracts
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome
Genotype-Phenotype Correlation for Nucleotide Substitutions in the IgII-IgIII Linker of FGFR2
Review: Genetics of Attention Deficit/Hyperactivity Disorder
Increased Prevalence of ADHD in Turner Syndrome with No Evidence of Imprinting Effects
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination
How a Hedgehog might see holoprosencephaly
Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21
The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly
A previously unidentified amino-terminal domain regulates transcriptional activity of wild-type and disease-associated human GLI2
Mutations in the human SIX3 gene in holoprosencephaly are loss of function
REPORTS
Mutations in the C-Terminal Domain of Sonic Hedgehog Cause Holoprosencephaly
A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22
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