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Results: 1-19 |
Results: 19
CHROMOSOME ANALYSIS GUIDELINES AND CYTOGENETIC QUALITY ASSESSMENT IN GERMANY
Authors: MILLER K HELD K MINY P
Citation: K. Miller et al., CHROMOSOME ANALYSIS GUIDELINES AND CYTOGENETIC QUALITY ASSESSMENT IN GERMANY, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 68-68
A RARE COMBINATION OF PARTIAL TRISOMY-9 A ND PULMONARY ATRESIA
Authors: NEKARDA T KECECIOGLU D KEHL HG GEHRMANN J MINY P VOGT J
Citation: T. Nekarda et al., A RARE COMBINATION OF PARTIAL TRISOMY-9 A ND PULMONARY ATRESIA, Klinische Padiatrie, 209(3), 1997, pp. 127-129
A NEW HERITABLE LIPID ABNORMALITY IN CHILDREN WITH PARTIAL SMITH-LEMLI-OPITZ SYNDROME PHENOTYPE
Authors: MESCHEDE D",SEEDORF,"SEEDORF U FOBKER M MINY P FLOTMANN U KOCH HG ULLRICH K ASSMANN G HORST J
Citation: U. Meschede D",seedorf,"seedorf et al., A NEW HERITABLE LIPID ABNORMALITY IN CHILDREN WITH PARTIAL SMITH-LEMLI-OPITZ SYNDROME PHENOTYPE, American journal of medical genetics, 68(3), 1997, pp. 5-5
EFFICIENCY OF PRENATAL DIAGNOSTIC METHODS AND PATIENT SELECTION CRITERIA
Authors: HOLZGREVE W TERCANLI S MINY P
Citation: W. Holzgreve et al., EFFICIENCY OF PRENATAL DIAGNOSTIC METHODS AND PATIENT SELECTION CRITERIA, Der Gynakologe, 29(7), 1996, pp. 565-572
PARENTAL ORIGIN OF THE EXTRA HAPLOID CHROMOSOME SET IN TRIPLOIDIES DIAGNOSED PRENATALLY
Authors: MINY P KOPPERS B DWORNICZAK B BOGDANOVA N HOLZGREVE W TERCANLI S BASARAN S REHDER H EXELER R HORST J
Citation: P. Miny et al., PARENTAL ORIGIN OF THE EXTRA HAPLOID CHROMOSOME SET IN TRIPLOIDIES DIAGNOSED PRENATALLY, American journal of medical genetics, 57(1), 1995, pp. 102-106
MATERNAL SERUM SCREENING FOR DETECTION OF FETAL CHROMOSOMAL-ANOMALIES
Authors: HOLZGREVE W MINY P SCHLOO R TERCANLI S
Citation: W. Holzgreve et al., MATERNAL SERUM SCREENING FOR DETECTION OF FETAL CHROMOSOMAL-ANOMALIES, Der Gynakologe, 28(5), 1995, pp. 280-288
CONGENITAL HEART-DISEASE IN THE 48,XXYY SYNDROME
Authors: MESCHEDE D NEKARDA T KECECIOGLU D LOSER H VOGT J MINY P HORST J
Citation: D. Meschede et al., CONGENITAL HEART-DISEASE IN THE 48,XXYY SYNDROME, Clinical genetics, 48(2), 1995, pp. 100-102
INDICATIONS AND METHODS FOR ANTENATAL CHROMOSOME ANALYSIS - MORE CHOICES REQUIRE MORE APPROPRIATE SELECTION
Authors: HOLZGREVE W GANSHIRTAHLERT D MINY P
Citation: W. Holzgreve et al., INDICATIONS AND METHODS FOR ANTENATAL CHROMOSOME ANALYSIS - MORE CHOICES REQUIRE MORE APPROPRIATE SELECTION, Current opinion in obstetrics & gynecology, 6(1), 1994, pp. 3-6
FETAL CELLS IN MATERNAL CIRCULATION THROUGHOUT GESTATION
Authors: GANSHIRT S GARRITSEN H MINY P HOLZGREVE W
Citation: S. Ganshirt et al., FETAL CELLS IN MATERNAL CIRCULATION THROUGHOUT GESTATION, Lancet, 343(8904), 1994, pp. 1038-1039
A NOVEL MUTATION IN EXON-8 OF THE PHENYLALANINE-HYDROXYLASE GENE IN THE POLISH POPULATION
Authors: ZYGULSKA M EIGEL A PIETRZYK JJ MINY P HORST J
Citation: M. Zygulska et al., A NOVEL MUTATION IN EXON-8 OF THE PHENYLALANINE-HYDROXYLASE GENE IN THE POLISH POPULATION, Human mutation, 2(1), 1993, pp. 74-76
DETECTION OF FETAL TRISOMY-21 AND TRISOMY-18 FROM MATERNAL BLOOD USING TRIPLE GRADIENT AND MAGNETIC CELL SORTING
Authors: GANSHIRTAHLERT D BORJESSONSTOLL R BURSCHYK M DOHR A GARRITSEN HSP HELMER E MINY P VELASCO M WALDE C PATTERSON D TENG N BHAT NM BIEBER MM HOLZGREVE W
Citation: D. Ganshirtahlert et al., DETECTION OF FETAL TRISOMY-21 AND TRISOMY-18 FROM MATERNAL BLOOD USING TRIPLE GRADIENT AND MAGNETIC CELL SORTING, American journal of reproductive immunology [1989], 30(2-3), 1993, pp. 194-201
INFLUENCE OF GENETICS ON PERINATAL MEDICI NE
Authors: HOLZGREVE W MINY P
Citation: W. Holzgreve et P. Miny, INFLUENCE OF GENETICS ON PERINATAL MEDICI NE, Archives of gynecology and obstetrics, 254(1-4), 1993, pp. 24-33
GENETIC-COUNSELING IN PRENATAL-DIAGNOSIS
Authors: HOLZGREVE W MINY P
Citation: W. Holzgreve et P. Miny, GENETIC-COUNSELING IN PRENATAL-DIAGNOSIS, European journal of obstetrics, gynecology, and reproductive biology, 49(3), 1993, pp. 125-129
PRENATAL-DIAGNOSIS AND MANAGEMENT OF FETAL HYDROCEPHALY AND LISSENCEPHALY
Authors: HOLZGREVE W FEIL R LOUWEN F MINY P
Citation: W. Holzgreve et al., PRENATAL-DIAGNOSIS AND MANAGEMENT OF FETAL HYDROCEPHALY AND LISSENCEPHALY, Child's nervous system, 9(7), 1993, pp. 408-412
GENETIC-FACTORS IN LISSENCEPHALY SYNDROMES - A REVIEW
Authors: MINY P HOLZGREVE W HORST J
Citation: P. Miny et al., GENETIC-FACTORS IN LISSENCEPHALY SYNDROMES - A REVIEW, Child's nervous system, 9(7), 1993, pp. 413-417
IMMEDIATE AND LONG-TERM APPLICATIONS OF TECHNOLOGY
Authors: HOLZGREVE W NIPPERT I GANSHIRTAHLERT D SCHLOO R MINY P
Citation: W. Holzgreve et al., IMMEDIATE AND LONG-TERM APPLICATIONS OF TECHNOLOGY, Clinical obstetrics and gynecology, 36(3), 1993, pp. 476-484
SUCCESSFUL NONINVASIVE PRENATAL-DIAGNOSIS OF FETAL ANEUPLOIDIES FROM MATERNAL CIRCULATION BY TRIPLE GRADIENT AND MAGNETIC ACTIVATED CELL SORTING - EVALUATION OF SPECIFICITY AND SENSITIVITY IN A LARGE SERIES OFPREGNANCIES
Authors: GANSHIRTAHLERT D BORJESSONSTOLL R BURSCHYK M GARRITSEN HSP MINY P NEUSSER M VELASCU M WALDE C HOLZGREVE W
Citation: D. Ganshirtahlert et al., SUCCESSFUL NONINVASIVE PRENATAL-DIAGNOSIS OF FETAL ANEUPLOIDIES FROM MATERNAL CIRCULATION BY TRIPLE GRADIENT AND MAGNETIC ACTIVATED CELL SORTING - EVALUATION OF SPECIFICITY AND SENSITIVITY IN A LARGE SERIES OFPREGNANCIES, American journal of human genetics, 53(3), 1993, pp. 249-249
PARENTAL ORIGIN OF THE SUPERNUMERARY CHROMOSOME SET IN TRIPLOIDS - MATERNAL ORIGIN AND PROLONGED INTRAUTERINE SURVIVAL
Authors: DWORNICZAK B KOPPERS B BOGDANOVA N HOLZGREVE W TERCANIL S HORST J MINY P
Citation: B. Dworniczak et al., PARENTAL ORIGIN OF THE SUPERNUMERARY CHROMOSOME SET IN TRIPLOIDS - MATERNAL ORIGIN AND PROLONGED INTRAUTERINE SURVIVAL, American journal of human genetics, 53(3), 1993, pp. 1403-1403
TESTING FOR FRAGILE X-SYNDROME IN 120 FAMILIES WITH A HISTORY OF MENTAL-RETARDATION
Authors: WITTWER B ZYGULSKA M MINY P EIGEL A HORST J
Citation: B. Wittwer et al., TESTING FOR FRAGILE X-SYNDROME IN 120 FAMILIES WITH A HISTORY OF MENTAL-RETARDATION, American journal of human genetics, 53(3), 1993, pp. 1513-1513
Risultati: 1-19 |