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Results: 1-14 |
Results: 14
ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM
Authors: KARADIMA G BUGGE M NICOLAIDIS P VASSILOPOULOS D AVRAMOPOULOS D GRIGORIADOU M ALBRECHT B PASSARGE E ANNEREN G BLENNOW E CLAUSEN N GALLAVOUMVOURAKI A TSEZOU A KITSIOUTZELI S HAHNEMANN JM HERTZ JM HOUGE G KUKLIK M MACEK M LACOMBE D MILLER K MONCLA A PAJARES IL PATSALIS PC PRIEUR M VEKEMANS M VONBEUST G BRONDUMNIELSEN K PETERSEN MB
Citation: G. Karadima et al., ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM, European journal of human genetics, 6(5), 1998, pp. 432-438
A CASE OF NON-FANCONI ANEMIA BONE-MARROW DYSFUNCTION WITH FAMILIAL INVOLVEMENT
Authors: PAPADOPOULOS NG PAPADAKI E KITSIOUTZELI S FARMAKAKIS T FRETZAYAS A
Citation: Ng. Papadopoulos et al., A CASE OF NON-FANCONI ANEMIA BONE-MARROW DYSFUNCTION WITH FAMILIAL INVOLVEMENT, Pediatric hematology and oncology, 15(3), 1998, pp. 277-281
DETECTION AND INCIDENCE OF CRYPTIC Y-CHROMOSOME SEQUENCES IN TURNER-SYNDROME PATIENTS
Authors: PATSALIS PC SISMANI C HADJIMARCOU MI KITSIOUTZELI S TZEZOU A HADJIATHANASIOU CG VELISSARIOU V LYMBERATOU E MOSCHONAS NK SKORDIS N
Citation: Pc. Patsalis et al., DETECTION AND INCIDENCE OF CRYPTIC Y-CHROMOSOME SEQUENCES IN TURNER-SYNDROME PATIENTS, Clinical genetics, 53(4), 1998, pp. 249-257
CLINICAL, CYTOGENETIC, AND MOLECULAR-GENETIC CHARACTERIZATION OF 2 UNRELATED PATIENTS WITH DUPLICATION OF 9P
Authors: SYRROU M KARADIMA G BLENNOW E TSEZOU A KITSIOUTZELI S GALLA A PETERSEN M PAGOULATOS G
Citation: M. Syrrou et al., CLINICAL, CYTOGENETIC, AND MOLECULAR-GENETIC CHARACTERIZATION OF 2 UNRELATED PATIENTS WITH DUPLICATION OF 9P, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 49-49
NONDISJUNCTION STUDIES IN TRISOMY-8
Authors: KARADIMA G AVRAMOPOULOS D GRIGORIADOU M PETERSEN MB ALBRECHT B ANNEREN G BLENNOW E BRONDUMNIELSEN K BUGGE M CLAUSEN N GALLAVOUMVOURAKI A HAHNEMANN JM HERTZ JM KITSIOUTZELI S LACOMBE D MILLER K MONCLA A PAJARES IL PASSARGE E PATSALIS PC PRIEUR M TSEZOU A VASSILOPOULOS D VEKEMANS M VONBEUST G
Citation: G. Karadima et al., NONDISJUNCTION STUDIES IN TRISOMY-8, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 105-105
SMCS IN PATIENTS WITH STIGMATA OF TURNER-SYNDROME ARE MOSTLY DERIVED FROM THE Y-CHROMOSOME - DNA AND FISH ANALYSIS
Authors: SISMANI C HADJIMARCOU MI STAVRIDES GS VELISSARIOU V KITSIOUTZELI S ZERA C LYBERATOU E TSEZOU A GALLA A SKORDIS N PATSALIS PC
Citation: C. Sismani et al., SMCS IN PATIENTS WITH STIGMATA OF TURNER-SYNDROME ARE MOSTLY DERIVED FROM THE Y-CHROMOSOME - DNA AND FISH ANALYSIS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 279-279
CLINICAL, CYTOGENETIC, AND MOLECULAR-GENETIC CHARACTERIZATION OF 2 UNRELATED PATIENTS WITH DUPLICATION OF 9P
Authors: SYRROU M KARADIMA G BLENNOW E TSEZOU A KITSIOUTZELI S GALLA A PETERSEN M PAGOULATOS G
Citation: M. Syrrou et al., CLINICAL, CYTOGENETIC, AND MOLECULAR-GENETIC CHARACTERIZATION OF 2 UNRELATED PATIENTS WITH DUPLICATION OF 9P, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 283-283
SUPERNUMERARY MARKER CHROMOSOMES (SMCS) IN TURNER-SYNDROME ARE MOSTLYDERIVED FROM THE Y-CHROMOSOME
Authors: PATSALIS PC HADJIMARCOU MI VELISSARIOU V KITSIOUTZELI S ZERA C SYRROU M LYBERATOU E TSEZOU A GALLA A SKORDIS N
Citation: Pc. Patsalis et al., SUPERNUMERARY MARKER CHROMOSOMES (SMCS) IN TURNER-SYNDROME ARE MOSTLYDERIVED FROM THE Y-CHROMOSOME, Clinical genetics, 51(3), 1997, pp. 184-190
ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM
Authors: KARADIMA G BUGGE M NICOLAIDIS P VASSILOPOULOS D VONBEUST G PAJARES IL ALBRECHT B ANNEREN G AVRAMOPOULOS D BLENNOW E BRONDUMNIELSEN K CLAUSEN N GALLAVOUMVOURAKI A GRIGORIADOU M HAHNEMANN JM HERTZ JM KITSIOUTZELI S LACOMBE D MILLER K MONCLA A PASSARGE E PATSALIS PC PRIEUR M TSEZOU A VEKEMANS M PETERSEN MB
Citation: G. Karadima et al., ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM, American journal of human genetics, 61(4), 1997, pp. 732-732
MOLECULAR CHARACTERIZATION OF DUPLICATION 9P
Authors: KITSIOUTZELI S BLENNOW E SYRROU M KARADIMA G TSEZOU A GALLA A PAGOULATOS G PETERSON MB
Citation: S. Kitsioutzeli et al., MOLECULAR CHARACTERIZATION OF DUPLICATION 9P, American journal of human genetics, 61(4), 1997, pp. 738-738
HIGH NITRATE CONTENT IN DRINKING-WATER - CYTOGENETIC EFFECTS IN EXPOSED CHILDREN
Authors: TSEZOU A KITSIOUTZELI S GALLA A GOURGIOTIS D PAPAGEORGIOU J MITROU S MOLYBDAS PA SINANIOTIS C
Citation: A. Tsezou et al., HIGH NITRATE CONTENT IN DRINKING-WATER - CYTOGENETIC EFFECTS IN EXPOSED CHILDREN, Archives of environmental health, 51(6), 1996, pp. 458-461
PARTIAL DISOMY OF XP AND THE PRESENCE OF SRY IN A PHENOTYPIC FEMALE
Authors: BAJALICA S BLENNOW E TSEZOU A GALLAVOUMVOURAKI A ALEVIZAKI M SINANIOTIS C KITSIOUTZELI S
Citation: S. Bajalica et al., PARTIAL DISOMY OF XP AND THE PRESENCE OF SRY IN A PHENOTYPIC FEMALE, Journal of Medical Genetics, 32(12), 1995, pp. 987-990
NONDISJUNCTION STUDIES IN TRISOMY-8
Authors: GRIGORIADOU M BUGGE M AVRAMOPOULOS D KITSIOUTZELI S ANNEREN G HERTZ JM LACOMBE D TSEZOU A GALLAVOUMVOURAKI A CLAUSEN N VASSILOPOULOS D BRONDUMNIELSEN K PETERSEN MB
Citation: M. Grigoriadou et al., NONDISJUNCTION STUDIES IN TRISOMY-8, American journal of human genetics, 57(4), 1995, pp. 639-639
CYTOGENETIC STUDIES IN CHILDREN ON LONG-TERM ANTICONVULSANT THERAPY
Authors: KITSIOUTZELI S GALLAVOUMVOURAKI A TSEZOU A KAVAZARAKIS E SKARDOUTSOU A KOUKOUTSAKIS P SINAMNIOTIS C
Citation: S. Kitsioutzeli et al., CYTOGENETIC STUDIES IN CHILDREN ON LONG-TERM ANTICONVULSANT THERAPY, Acta paediatrica, 83(6), 1994, pp. 672-673
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