Morava E - Search Results

1

Clinical and genetic heterogeneity in frontometaphyseal dysplasia: severe progressive scoliosis in two families.

Morava E, Illés T, Weisenbach J, Kárteszi J, Kosztolányi G. Morava E, et al. Am J Med Genet A. 2003 Jan 30;116A(3):272-7. doi: 10.1002/ajmg.a.10831. Am J Med Genet A. 2003. PMID: 12503106

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

De novo partial duplication of long arm of chromosome 13: dup(13)(q12-->q14).

Hermann R, Soltész G, Morava E, Kosztolányi G, Czakó M. Hermann R, et al. Among authors: morava e. Am J Med Genet. 2000 Jun 5;92(4):296-7. Am J Med Genet. 2000. PMID: 10842301 No abstract available.

8

[22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot].

Morava E, Masszi G, Czakó M, Tóth G, Melegh B, Kosztolányi G. Morava E, et al. Orv Hetil. 2000 Aug 20;141(34):1873-5. Orv Hetil. 2000. PMID: 11006712 Hungarian.

9

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

10

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.

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