Morava E - Search Results

1

Presenile cataract: consider cholestanol.

Tészás A, Pfund Z, Morava E, Kosztolányi G, Sistermans E, Wevers RA, Kellermayer R. Tészás A, et al. Among authors: morava e. Arch Ophthalmol. 2006 Oct;124(10):1490-2. doi: 10.1001/archopht.124.10.1490. Arch Ophthalmol. 2006. PMID: 17030721 No abstract available.

2

X-linked mental retardation syndrome: three brothers with the Brooks-Wisniewski-Brown syndrome.

Morava E, Storcz J, Kosztolányi G. Morava E, et al. Am J Med Genet. 1996 Jul 12;64(1):59-62. doi: 10.1002/(SICI)1096-8628(19960712)64:1<59::AID-AJMG8>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8826449

3

[Alpha thalassemia/metal retardation syndrome--a new X-chromosome linked recessive genetically inherited symptom complex].

Morava E, Kosztolányi G. Morava E, et al. Orv Hetil. 1996 Dec 15;137(50):2799-801. Orv Hetil. 1996. PMID: 9679615 Hungarian.

4

[Molecular biologic screening test (PCR) for fragile X syndrome].

Kovács E, Morava E, Nádasi E, Czakó M, Melegh B, Kosztolányi G. Kovács E, et al. Among authors: morava e. Orv Hetil. 1998 Dec 27;139(52):3121-3. Orv Hetil. 1998. PMID: 9914733 Review. Hungarian.

5

Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population.

Gyürüs P, Molnár J, Melegh B, Tóth G, Morava E, Kosztolányi G, Méhes K. Gyürüs P, et al. Among authors: morava e. Am J Med Genet. 1999 Nov 26;87(3):245-50. doi: 10.1002/(sici)1096-8628(19991126)87:3<245::aid-ajmg9>3.3.co;2-5. Am J Med Genet. 1999. PMID: 10564878

6

Isodicentric Y chromosome in an Ullrich-Turner patient without virilization.

Morava E, Hermann R, Czakó M, Soltész G, Kosztolányi G. Morava E, et al. Am J Med Genet. 2000 Mar 13;91(2):99-101. doi: 10.1002/(sici)1096-8628(20000313)91:2<99::aid-ajmg3>3.0.co;2-c. Am J Med Genet. 2000. PMID: 10748405

7

Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian children.

Morava E, Czakó M, Melegh B, Kosztolányi G. Morava E, et al. Clin Genet. 2000 Nov;58(5):403-5. doi: 10.1034/j.1399-0004.2000.580512.x. Clin Genet. 2000. PMID: 11140842

8

Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies.

Riegel M, Morava E, Czakó M, Kosztolányi G, Schinzel A. Riegel M, et al. Among authors: morava e. Am J Med Genet. 2001 Aug 15;102(3):227-30. doi: 10.1002/ajmg.1455. Am J Med Genet. 2001. PMID: 11484198 Review.

9

[Mucolipidosis II with unusual biochemical parameters].

Morava E, Eduard P, Tóth G, Dobos M, Melegh B, Kosztolányi G. Morava E, et al. Orv Hetil. 2002 Jan 20;143(3):135-7. Orv Hetil. 2002. PMID: 11883111 Hungarian.

10

Patient with rheumatoid arthritis and MCA/MR syndrome due to unbalanced der(18) transmission of a paternal translocation t(18;20)(p11.1;p11.1).

Czakó M, Riegel M, Morava E, Schinzel A, Kosztolányi G. Czakó M, et al. Among authors: morava e. Am J Med Genet. 2002 Mar 15;108(3):226-8. doi: 10.1002/ajmg.10243. Am J Med Genet. 2002. PMID: 11891691

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