Partial craniosynostosis in a patient with deletion 22q11 [2]

Judit Karteszi, W. Kress, M. Szasz, M. Czako, B. Melegh, G. Kosztolányi, E. Morava

Research output: Contribution to journalArticle

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)481-483
Number of pages3
JournalGenetic Counseling
Volume15
Issue number4
Publication statusPublished - 2004

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Receptor, Fibroblast Growth Factor, Type 3
Receptor, Fibroblast Growth Factor, Type 2
Receptor, Fibroblast Growth Factor, Type 1
Chromosomes, Human, Pair 22
Fibroblast Growth Factor Receptors
Craniosynostoses
Chromosome Deletion
Receptor Protein-Tyrosine Kinases
Point Mutation
Premature Infants
Protein-Tyrosine Kinases
Newborn Infant

ASJC Scopus subject areas

  • Genetics(clinical)

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Karteszi, J., Kress, W., Szasz, M., Czako, M., Melegh, B., Kosztolányi, G., & Morava, E. (2004). Partial craniosynostosis in a patient with deletion 22q11 [2]. Genetic Counseling, 15(4), 481-483.

Partial craniosynostosis in a patient with deletion 22q11 [2]. / Karteszi, Judit; Kress, W.; Szasz, M.; Czako, M.; Melegh, B.; Kosztolányi, G.; Morava, E.

In: Genetic Counseling, Vol. 15, No. 4, 2004, p. 481-483.

Research output: Contribution to journalArticle

Karteszi, J, Kress, W, Szasz, M, Czako, M, Melegh, B, Kosztolányi, G & Morava, E 2004, 'Partial craniosynostosis in a patient with deletion 22q11 [2]', Genetic Counseling, vol. 15, no. 4, pp. 481-483.
Karteszi, Judit ; Kress, W. ; Szasz, M. ; Czako, M. ; Melegh, B. ; Kosztolányi, G. ; Morava, E. / Partial craniosynostosis in a patient with deletion 22q11 [2]. In: Genetic Counseling. 2004 ; Vol. 15, No. 4. pp. 481-483.
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