Czako M - Search Results

1

Partial craniosynostosis in a patient with deletion 22q11.

Karteszi J, Kress W, Szasz M, Czako M, Melegh B, Kosztolanyi GY, Morava E. Karteszi J, et al. Among authors: czako m. Genet Couns. 2004;15(4):481-3. Genet Couns. 2004. PMID: 15658627 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

[Vascular diseases, spina bifida and schizophrenia in a single family associated with the heterozygote mutation of the heat-sensitive variant of methylenetetrahydrofolate reductase].

Horváth A, Morava E, Tóth G, Czakó M, Melegh B, Kosztolányi G. Horváth A, et al. Among authors: czako m. Orv Hetil. 2001 Jul 8;142(27):1445-8. Orv Hetil. 2001. PMID: 11481907 Hungarian.

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: 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.

9

[Kennedy disease in a patient with progressive speech disorder].

Kárteszi J, Morava E, Czakó M, Gáti I, Czopf J, Kosztolányi G, Melegh B. Kárteszi J, et al. Among authors: czako m. Orv Hetil. 2001 Sep 2;142(35):1915-7. Orv Hetil. 2001. PMID: 11601179 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. 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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