Kosztolányi G - Search Results

1

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

2

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: kosztolanyi g. 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

3

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: kosztolanyi g. Clin Genet. 2000 Nov;58(5):403-5. doi: 10.1034/j.1399-0004.2000.580512.x. Clin Genet. 2000. PMID: 11140842

4

Mosaic supernumerary ring chromosome 1 in a three-generational family: 10-year follow-up report.

Kosztolányi G, Brecevic L, Bajnòczky K, Schinzel A, Riegel M. Kosztolányi G, et al. Eur J Med Genet. 2011 Mar-Apr;54(2):152-6. doi: 10.1016/j.ejmg.2010.11.015. Epub 2010 Dec 9. Eur J Med Genet. 2011. PMID: 21145991

5

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: kosztolanyi gy. Genet Couns. 2002;13(4):455-7. Genet Couns. 2002. PMID: 12558117

6

A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion.

Morava E, Bartsch O, Czako M, Frensel A, Kárteszi J, Kosztolányi GY. Morava E, et al. Among authors: kosztolanyi gy. Genet Couns. 2003;14(3):337-42. Genet Couns. 2003. PMID: 14577679

7

Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus.

Kotzot D, Bernasconi F, Brecevic L, Robinson WP, Kiss P, Kosztolanyi G, Lurie IW, Superti-Furga A, Schinzel A. Kotzot D, et al. Among authors: kosztolanyi g. Eur J Pediatr. 1995 Jun;154(6):477-82. doi: 10.1007/BF02029360. Eur J Pediatr. 1995. PMID: 7545578

8

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

Morava E, Storcz J, Kosztolányi G. Morava E, et al. Among authors: kosztolanyi g. 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

9

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

10

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: kosztolanyi gy. Genet Couns. 2004;15(4):481-3. Genet Couns. 2004. PMID: 15658627 No abstract available.

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