Authors:
PAJOR L
SZUHAI K
MEHES G
KOSZTOLANYI G
JAKSO P
LENDVAI G
SZANYI I
KAJTAR P
Citation: L. Pajor et al., COMBINED METAPHASE, INTERPHASE CYTOGENETIC, AND FLOW CYTOMETRIC ANALYSIS OF DNA CONTENT OF PEDIATRIC ACUTE LYMPHOBLASTIC-LEUKEMIA, Cytometry, 34(2), 1998, pp. 87-94
Citation: G. Kosztolanyi, LEPRECHAUNISM DONOHUE-SYNDROME INSULIN-RECEPTOR GENE-MUTATIONS - A SYNDROME DELINEATION STORY FROM CLINICOPATHOLOGICAL DESCRIPTION TO MOLECULAR UNDERSTANDING, European journal of pediatrics, 156(4), 1997, pp. 253-255
Citation: G. Kosztolanyi et al., INCREASE IN THE RATE OF MOSAICISM AND DISEASE SEVERITY IN SUCCESSIVE GENERATIONS - CYTOGENETIC ANTICIPATION, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 107-107
Citation: Ep. Tardy et al., PRENATAL EXCLUSION OF SEGMENTAL TRISOMY IN FAMILIAL CHROMOSOME-21 PERICENTRIC-INVERSION BY FLUORESCENCE IN-SITU HYBRIDIZATION, Prenatal diagnosis, 17(9), 1997, pp. 871-873
Citation: E. Morava et al., X-LINKED MENTAL-RETARDATION SYNDROME - 3 BROTHERS WITH THE BROOKS-WISNIEWSKI-BROWN-SYNDROME, American journal of medical genetics, 64(1), 1996, pp. 59-62
Citation: G. Kosztolanyi et al., MILD CF IN A DELTA-F508 R347H COMPOUND HETEROZYGOTE WOMAN - DOES THE MANIFESTATION OF THIS GENOTYPE DIFFER IN THE 2 SEXES/, Clinical genetics, 49(2), 1996, pp. 103-105
Authors:
KOTZOT D
BERNASCONI F
BRECEVIC L
ROBINSON WP
KISS P
KOSZTOLANYI G
LURIE IW
SUPERTIFURGA A
SCHINZEL A
Citation: D. Kotzot et al., PHENOTYPE OF THE WILLIAMS-BEUREN SYNDROME-ASSOCIATED WITH HEMIZYGOSITY AT THE ELASTIN LOCUS, European journal of pediatrics, 154(6), 1995, pp. 477-482
Citation: G. Kosztolanyi et al., SYNDROME OF ARACHNODACTYLY, DISTURBANCE OF CRANIAL OSSIFICATION, PROTRUDING EYES, FEEDING DIFFICULTIES, AND MENTAL-RETARDATION, American journal of medical genetics, 58(3), 1995, pp. 213-216