Muenke M - Search Results

1

Introduction to the American Journal of Medical Genetics Part C on holoprosencephaly.

Muenke M, Solomon BD, Odent S. Muenke M, et al. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):1-2. doi: 10.1002/ajmg.c.30255. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104593 No abstract available.

2

Holoprosencephaly: a paradigm for the complex genetics of brain development.

Roessler E, Muenke M. Roessler E, et al. Among authors: muenke m. J Inherit Metab Dis. 1998 Aug;21(5):481-97. doi: 10.1023/a:1005406719292. J Inherit Metab Dis. 1998. PMID: 9728329 Review.

3

Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1).

Roessler E, Mittaz L, Du Y, Scott HS, Chang J, Rossier C, Guipponi M, Matsuda SP, Muenke M, Antonarakis SE. Roessler E, et al. Among authors: muenke m. Hum Genet. 1999 Nov;105(5):489-95. doi: 10.1007/s004390051135. Hum Genet. 1999. PMID: 10598817

4

The molecular genetics of holoprosencephaly: a model of brain development for the next century.

Roessler E, Muenke M. Roessler E, et al. Among authors: muenke m. Childs Nerv Syst. 1999 Nov;15(11-12):646-51. doi: 10.1007/s003810050453. Childs Nerv Syst. 1999. PMID: 10603005 Review.

5

Genetics of ventral forebrain development and holoprosencephaly.

Muenke M, Beachy PA. Muenke M, et al. Curr Opin Genet Dev. 2000 Jun;10(3):262-9. doi: 10.1016/s0959-437x(00)00084-8. Curr Opin Genet Dev. 2000. PMID: 10826992 Review.

6

Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.

Brown LY, Odent S, David V, Blayau M, Dubourg C, Apacik C, Delgado MA, Hall BD, Reynolds JF, Sommer A, Wieczorek D, Brown SA, Muenke M. Brown LY, et al. Among authors: muenke m. Hum Mol Genet. 2001 Apr 1;10(8):791-6. doi: 10.1093/hmg/10.8.791. Hum Mol Genet. 2001. PMID: 11285244

7

Genetics of population isolates.

Arcos-Burgos M, Muenke M. Arcos-Burgos M, et al. Among authors: muenke m. Clin Genet. 2002 Apr;61(4):233-47. doi: 10.1034/j.1399-0004.2002.610401.x. Clin Genet. 2002. PMID: 12030885 Review.

8

The decision to continue: the experiences and needs of parents who receive a prenatal diagnosis of holoprosencephaly.

Redlinger-Grosse K, Bernhardt BA, Berg K, Muenke M, Biesecker BB. Redlinger-Grosse K, et al. Among authors: muenke m. Am J Med Genet. 2002 Nov 1;112(4):369-78. doi: 10.1002/ajmg.10657. Am J Med Genet. 2002. PMID: 12376939

9

Multiple hits during early embryonic development: digenic diseases and holoprosencephaly.

Ming JE, Muenke M. Ming JE, et al. Among authors: muenke m. Am J Hum Genet. 2002 Nov;71(5):1017-32. doi: 10.1086/344412. Epub 2002 Oct 22. Am J Hum Genet. 2002. PMID: 12395298 Free PMC article. Review. No abstract available.

10

The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephaly.

Karkera JD, Izraeli S, Roessler E, Dutra A, Kirsch I, Muenke M. Karkera JD, et al. Among authors: muenke m. Cytogenet Genome Res. 2002;97(1-2):62-7. doi: 10.1159/000064057. Cytogenet Genome Res. 2002. PMID: 12438740

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