Czakó M - Search Results

1

A cryptic unbalanced translocation resulting in del 13q and dup 15q.

Tészás A, Møller RS, Kellermayer R, Czakó M, Kjaer KW, Ullmann R, Melegh B, Tommerup N, Kosztolányi G. Tészás A, et al. Among authors: czako m. Am J Med Genet A. 2008 Oct 1;146A(19):2570-3. doi: 10.1002/ajmg.a.32394. Am J Med Genet A. 2008. PMID: 18792978 No abstract available.

2

[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: czako m. Orv Hetil. 1998 Dec 27;139(52):3121-3. Orv Hetil. 1998. PMID: 9914733 Review. Hungarian.

3

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

Morava E, Hermann R, Czakó M, Soltész G, Kosztolányi G. Morava E, et al. Among authors: czako m. 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

4

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: czako m. Am J Med Genet. 2000 Jun 5;92(4):296-7. Am J Med Genet. 2000. PMID: 10842301 No abstract available.

5

[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. Among authors: czako m. Orv Hetil. 2000 Aug 20;141(34):1873-5. Orv Hetil. 2000. PMID: 11006712 Hungarian.

6

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

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

7

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: czako m. Am J Med Genet. 2001 Aug 15;102(3):227-30. doi: 10.1002/ajmg.1455. Am J Med Genet. 2001. PMID: 11484198 Review.

8

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. Am J Med Genet. 2002 Mar 15;108(3):226-8. doi: 10.1002/ajmg.10243. Am J Med Genet. 2002. PMID: 11891691

9

Tissue specific mosaicism of trisomy 9 in a patient with severe torsion scoliosis.

Morava E, Czakó M, Aszmann M, Illés T, Kosztolányi GY. Morava E, et al. Among authors: czako m. Genet Couns. 2002;13(4):455-7. Genet Couns. 2002. PMID: 12558117

10

Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotonia.

Morava E, Bartsch O, Czakó M, Frensel A, Kalscheuer V, Kárteszi J, Kosztolányi G. Morava E, et al. Among authors: czako m. Clin Dysmorphol. 2003 Apr;12(2):123-7. doi: 10.1097/01.mcd.0000059768.40218.9b. Clin Dysmorphol. 2003. PMID: 12868476

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