UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

The association between an abnormal nuchal skin fold, trisomy 21, and ultrasound abnormalities identified during the second trimester of pregnancy

Ultrasound in obstetrics & gynecology, 1993-11, Vol.3 (6), p.387-394

1993

Volltextzugriff (PDF)

Evidence for genetic control of nondisjunction in man

American journal of human genetics, 1980-07, Vol.32 (4), p.477-483

1980

Volltextzugriff (PDF)

The use of color Doppler ultrasound to identify fetuses at increased risk for trisomy 21: an alternative for high-risk patients who decline genetic amniocentesis

Obstetrics and gynecology (New York. 1953), 1995-03, Vol.85 (3), p.378-386

1995

Volltextzugriff (PDF)

Optical Studies of the interaction of 4'-6'-diamidino-2-phenylindole with DNA and metaphase chromosomes

Chromosoma, 1977-03, Vol.60 (1), p.15-25

1977

Volltextzugriff (PDF)

Correlation Between Prognosis and Bone Marrow Chromosomal Patterns in Children With Acute Nonlymphocytic Leukemia: Similarities and Differences Compared to Adults

Blood, 1979-10, Vol.54 (4), p.818-823

1979

Volltextzugriff (PDF)

Detection of sister chromatid exchanges by 4'-6-diamidino-2-phenylindole fluorescence

Chromosoma, 1976-01, Vol.57 (3), p.219-225

1976

Volltextzugriff (PDF)

Partial Trisomy of the Long Arm of Chromosome No. 7

Journal of medical genetics, 1973-06, Vol.10 (2), p.187-189

1973

Volltextzugriff (PDF)

Genetic Disorders in Adolescents and Young Adults

The Pediatric clinics of North America, 1973-12, Vol.20 (4), p.865-872

Alfi, Omar S.

1973

Volltextzugriff (PDF)

Performing cytogenetic studies on ascitic, amniotic and hygroma fluid

Journal of reproductive medicine, 1990-12, Vol.35 (12), p.1145

1990

Volltextzugriff (PDF)

Variation in lateral asymmetry of human chromosome 1

Cytogenetic and genome research, 1978-01, Vol.21 (5), p.243-250

1978

Volltextzugriff (PDF)

Double Autosomal Trisomy and Mosaicism for Chromosomes No. 8 and No. 21

Journal of medical genetics, 1974-03, Vol.11 (1), p.96-101

1974

Volltextzugriff (PDF)

Ambiguous genitalia in XX male children: report of two infants

Pediatrics (Evanston), 1977-07, Vol.60 (1), p.55-59

1977

Volltextzugriff (PDF)

Tuberculin Sensitivity in Kuwaiti Schools

BMJ, 1958-04, Vol.1 (5075), p.870-871

Alfi, Omar

1958

Volltextzugriff (PDF)

A family with a large Y chromosome

Journal of medical genetics, 1970-03, Vol.7 (1), p.37-40

el-Alfi, O S

1970

Volltextzugriff (PDF)

Chromosome fragility and susceptibility of Bloom's syndrome fibroblasts to SV40 transformation

Experientia, 1980-03, Vol.36 (3), p.296-297

1980

Volltextzugriff (PDF)

Detection of lateral asymmetry in the C band of human chromosomes by BrdU-DAPI fluorescence

Somatic Cell Genetics, 1978-09, Vol.4 (5), p.603-608

1978

Volltextzugriff (PDF)

CHROMOSOME POLYMORPHISM AND PRENATAL DIAGNOSIS

The Lancet (British edition), 1975-05, Vol.305 (7918), p.1253-1253

1975

Volltextzugriff (PDF)

Regional mapping of the gene for human UDPGal 4-epimerase on chromosome 1 in mouse-human hybrids

Cytogenetic and genome research, 1979-01, Vol.24 (4), p.217-223

1979

Volltextzugriff (PDF)

Quinacrine fluoromicroscopy in the identification of human mitotic chromosomes

Pediatrics (Evanston), 1971-09, Vol.48 (3), p.423-425

1971

Volltextzugriff (PDF)

False negative maternal serum alpha-fetoprotein determinations in myelodysplasia: The role of ultrasound

American journal of obstetrics and gynecology, 1982-10, Vol.144 (3), p.352-355

1982

Volltextzugriff (PDF)

Length variation in the quinacrine-binding segment of human Y chromosomes of different sizes

Cytogenetic and genome research, 1971-01, Vol.10 (3), p.190-198

1971

Volltextzugriff (PDF)

A rapid C-band staining technique for chromosomes

The Journal of laboratory and clinical medicine, 1973-10, Vol.82 (4), p.692

1973

Volltextzugriff (PDF)

Differential fluorescence of sister chromatids with 4'-6-diamidino-2-phenylindole

Canadian journal of genetics and cytology, 1976-09, Vol.18 (3), p.545-547

1976

Volltextzugriff (PDF)

Maternofetal transfusion: Immunologic and cytogenetic evidence

American journal of obstetrics and gynecology, 1969-01, Vol.103 (4), p.599-600

1969

Volltextzugriff (PDF)

IMMUNOLOGICAL ASPERMATOGENESIS IN MAN

Reproduction (Cambridge, England), 1970-02, Vol.21 (1), p.23-28

1970

Volltextzugriff (PDF)

1 – 25 von 176

Menü

Weitere Dienste

Einstellungen

The association between an abnormal nuchal skin fold, trisomy 21, and ultrasound abnormalities identified during the second trimester of pregnancy

Evidence for genetic control of nondisjunction in man

The use of color Doppler ultrasound to identify fetuses at increased risk for trisomy 21: an alternative for high-risk patients who decline genetic amniocentesis

Optical Studies of the interaction of 4'-6'-diamidino-2-phenylindole with DNA and metaphase chromosomes

Correlation Between Prognosis and Bone Marrow Chromosomal Patterns in Children With Acute Nonlymphocytic Leukemia: Similarities and Differences Compared to Adults

Detection of sister chromatid exchanges by 4'-6-diamidino-2-phenylindole fluorescence

Partial Trisomy of the Long Arm of Chromosome No. 7

Genetic Disorders in Adolescents and Young Adults

Performing cytogenetic studies on ascitic, amniotic and hygroma fluid

Variation in lateral asymmetry of human chromosome 1

Double Autosomal Trisomy and Mosaicism for Chromosomes No. 8 and No. 21

Ambiguous genitalia in XX male children: report of two infants

Tuberculin Sensitivity in Kuwaiti Schools

A family with a large Y chromosome

Chromosome fragility and susceptibility of Bloom's syndrome fibroblasts to SV40 transformation

Detection of lateral asymmetry in the C band of human chromosomes by BrdU-DAPI fluorescence

CHROMOSOME POLYMORPHISM AND PRENATAL DIAGNOSIS

Regional mapping of the gene for human UDPGal 4-epimerase on chromosome 1 in mouse-human hybrids

Quinacrine fluoromicroscopy in the identification of human mitotic chromosomes

False negative maternal serum alpha-fetoprotein determinations in myelodysplasia: The role of ultrasound

Length variation in the quinacrine-binding segment of human Y chromosomes of different sizes

A rapid C-band staining technique for chromosomes

Differential fluorescence of sister chromatids with 4'-6-diamidino-2-phenylindole

Maternofetal transfusion: Immunologic and cytogenetic evidence

IMMUNOLOGICAL ASPERMATOGENESIS IN MAN

Suchergebnisse filtern