Münke M - Search Results

1

Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature.

Münke M, Kruse K, Goos M, Ropers HH, Tolksdorf M. Münke M, et al. Eur J Pediatr. 1983 Oct;141(1):8-13. doi: 10.1007/BF00445661. Eur J Pediatr. 1983. PMID: 6580169

2

[Psychometric results in patients with Klinefelter syndrome].

Gutezeit G, Münke M, Tolksdorf M. Gutezeit G, et al. Among authors: munke m. Monatsschr Kinderheilkd. 1982 Aug;130(8):613-5. Monatsschr Kinderheilkd. 1982. PMID: 7133016 German.

3

Forebrain cleavage gene causing holoprosencephaly: deletion mapping to chromosome band 2p21.

Hecht BK, Hecht F, Münke M. Hecht BK, et al. Among authors: munke m. Am J Med Genet. 1991 Jul 1;40(1):130. doi: 10.1002/ajmg.1320400131. Am J Med Genet. 1991. PMID: 1887845 No abstract available.

4

Oral-facial-digital syndrome type VI (Váradi syndrome): further clinical delineation.

Münke M, McDonald DM, Cronister A, Stewart JM, Gorlin RJ, Zackai EH. Münke M, et al. Am J Med Genet. 1990 Mar;35(3):360-9. doi: 10.1002/ajmg.1320350310. Am J Med Genet. 1990. PMID: 2309783

5

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly.

Münke M. Münke M. Am J Med Genet. 1989 Oct;34(2):237-45. doi: 10.1002/ajmg.1320340222. Am J Med Genet. 1989. PMID: 2683787 Review. No abstract available.

6

Partial physical map of human chromosome 21.

Gardiner K, Watkins P, Münke M, Drabkin H, Jones C, Patterson D. Gardiner K, et al. Among authors: munke m. Somat Cell Mol Genet. 1988 Nov;14(6):623-37. doi: 10.1007/BF01535316. Somat Cell Mol Genet. 1988. PMID: 3194801

7

Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male.

Münke M, Page DC, Brown LG, Armson BA, Zackai EH, Mennuti MT, Emanuel BS. Münke M, et al. Hum Genet. 1988 Nov;80(3):219-23. doi: 10.1007/BF01790089. Hum Genet. 1988. PMID: 3192211

8

Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature.

Münke M, Emanuel BS, Zackai EH. Münke M, et al. Am J Med Genet. 1988 Aug;30(4):929-38. doi: 10.1002/ajmg.1320300409. Am J Med Genet. 1988. PMID: 3055987 Review.

9

Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes.

Münke M, Foellmer B, Watkins PC, Cowan JM, Carroll AJ, Gusella JF, Francke U. Münke M, et al. Am J Hum Genet. 1988 Apr;42(4):542-9. Am J Hum Genet. 1988. PMID: 3348217 Free PMC article.

10

The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17.

Münke M, Kraus JP, Ohura T, Francke U. Münke M, et al. Am J Hum Genet. 1988 Apr;42(4):550-9. Am J Hum Genet. 1988. PMID: 2894761 Free PMC article.

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