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Results:
1-14
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Results: 14
Authors:
FRYSSIRA H
SOFOCLEOUS C
KOLIALEXI A
ZOGRAFOU G
CHATZISEVASTOU C
MAVROU A
METAXOTOU C
Citation: H. Fryssira et al., 46,XY,DEL(2) (Q32-QTER) IN A FEMALE WITH MULTIPLE CONGENITAL-ABNORMALITIES, European journal of human genetics, 6, 1998, pp. 2066-2066
DETECTION OF FETAL NRBCS FROM MATERNAL BLOOD BY 2-STEP ENRICHMENT USING MAGNETIC CELL SORTING (MACS)
Authors:
MAVROU A
KOLIALEXI A
TSAGARIS G
PAPADOPOULOU E
ANTSAKLIS A
METAXOTOU C
Citation: A. Mavrou et al., DETECTION OF FETAL NRBCS FROM MATERNAL BLOOD BY 2-STEP ENRICHMENT USING MAGNETIC CELL SORTING (MACS), European journal of human genetics, 6, 1998, pp. 6036-6036
Authors:
KOLIALEXI A
MAVROU A
TSENGHI C
TSANGARIS GT
DAFERMOU E
TZORTZATOU F
POLYCHRONOPOULOU S
HAIDAS S
METAXOTOU C
Citation: A. Kolialexi et al., CHROMOSOME FRAGILITY AND PREDISPOSITION TO CHILDHOOD MALIGNANCIES, Anticancer research, 18(4A), 1998, pp. 2359-2364
Authors:
MAVROU A
METAXOTOU C
TRICHOPOULOS D
Citation: A. Mavrou et al., AWARENESS AND USE OF PRENATAL-DIAGNOSIS AMONG GREEK WOMEN - A NATIONAL SURVEY, Prenatal diagnosis, 18(4), 1998, pp. 349-355
Authors:
DACOUVOUTETAKIS C
KARAVANAKIKARANASSIOU K
PETROU V
GEORGOPOULOS N
MANIATICHRISTIDI M
MAVROU A
Citation: C. Dacouvoutetakis et al., THE GROWTH-PATTERN AND FINAL HEIGHT OF GIRLS WITH TURNER-SYNDROME WITH AND WITHOUT HUMAN GROWTH-HORMONE TREATMENT, Pediatrics, 101(4), 1998, pp. 663-668
Authors:
METAXOTOU C
MAVROU A
ANTSAKLIS A
Citation: C. Metaxotou et al., PRENATAL-DIAGNOSIS SERVICES IN GREECE, European journal of human genetics, 5, 1997, pp. 39-41
Authors:
MAVROU A
KOLIALEXI A
ANTSAKLIS A
METAXOTOU C
Citation: A. Mavrou et al., FETAL CELL ISOLATION FROM MATERNAL BLOOD-SAMPLES USING MACS, IMMUNOPHENOTYPING AND FISH, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 165-165
Authors:
KOLIALEXI A
FRYSSIRA H
MAVROU A
TZIROPOULOU M
Citation: A. Kolialexi et al., UNUSUAL SUPERNUMERARY CHROMOSOME IN A PATIENT RESULTING FROM A MATERNAL RECIPROCAL 11Q 22Q TRANSLOCATION/, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 238-238
Authors:
SOFOCLEOUS C
KALAITSIDAKI M
MAVROU A
METAXOTOU C
KATTAMIS C
Citation: C. Sofocleous et al., MOLECULAR ANALYSIS OF THE FMR-1 GENE IN MENTALLY-RETARDED GREEK CHILDREN, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 280-280
Authors:
MAVROU A
ZHENG YL
KOLIALEXI A
METAXOTOU C
BIANCHI DW
Citation: A. Mavrou et al., FETAL NUCLEATED ERYTHROCYTES (NRBCS) IN CHORIONIC VILLUS SAMPLE SUPERNATANT FLUIDS - AN ADDITIONAL SOURCE OF FETAL MATERIAL FOR KARYOTYPE CONFIRMATION, Prenatal diagnosis, 17(7), 1997, pp. 643-649
Authors:
POLYCHRONOPOULOU S
PANAGIOTOU JP
PAPADAKIS T
MAVROU A
ANAGNOSTOU D
HAIDAS S
Citation: S. Polychronopoulou et al., SECONDARY MALIGNANCIES IN A CHILD WITH HODGKINS-DISEASE - PERIPHERAL T-CELL LYMPHOMA AND MYELODYSPLASTIC SYNDROME EVOLVING INTO ACUTE NONLYMPHOBLASTIC LEUKEMIA, Medical and pediatric oncology, 26(5), 1996, pp. 359-366
Authors:
FLORENTIN L
BILL C
KEKOU K
TRIPODIS N
MAVROU A
METAXOTOU C
Citation: L. Florentin et al., MAPPING DYSTROPHIN GENE RECOMBINANTS IN GREEK DMD BMD FAMILIES - LOW RECOMBINATION FREQUENCIES IN THE STR REGION/, Human genetics, 96(4), 1995, pp. 423-426
Authors:
FLORENTIN L
MAVROU A
KEKOU K
METAXOTOU C
Citation: L. Florentin et al., DELETION PATTERNS OF DUCHENNE AND BECKER MUSCULAR-DYSTROPHIES IN GREECE, Journal of Medical Genetics, 32(1), 1995, pp. 48-51
Authors:
KALAITSIDAKI M
MAVROU A
SALAVOURA K
METAXOTOU C
Citation: M. Kalaitsidaki et al., MOLECULAR STUDIES OF PRADER-WILLI AND ANGELMAN SYNDROME PATIENTS USING MICROSATELLITES FROM CHROMOSOME-15, American journal of human genetics, 53(3), 1993, pp. 1179-1179
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