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...

Increased Sylvian fissure angle as early sonographic sign of malformation of cortical development

Ultrasound in obstetrics & gynecology, 2019-08, Vol.54 (2), p.199-206

2019

Volltextzugriff (PDF)

OC18.04: Interhemispheric opening of fetal brain by 3D neurosonography: physiological change and a gourd sign in MCD cases

Ultrasound in obstetrics & gynecology, 2020-10, Vol.56 (S1), p.51-51

2020

Volltextzugriff (PDF)

VP28.06: Which fetuses are indicated for prenatal‐targeted exome sequencing testing? Increased NT or structural anomalies?

Ultrasound in obstetrics & gynecology, 2021-10, Vol.58 (S1), p.213-214

2021

Volltextzugriff (PDF)

P20.01: Low‐set ear detected by three‐dimensional ultrasound in the first trimester and genetic cause

Ultrasound in obstetrics & gynecology, 2018-10, Vol.52 (S1), p.190-191

2018

Volltextzugriff (PDF)

EP08.07: Measurement of Sylvian fissure angles at 18–30 weeks' gestation in cases with neuronal migration disorder

Ultrasound in obstetrics & gynecology, 2018-10, Vol.52 (S1), p.223-223

2018

Volltextzugriff (PDF)

EP08.08: Ventricular occupying ratio at 18–30 weeks' gestation: normal reference range and ventriculomegaly

Ultrasound in obstetrics & gynecology, 2018-10, Vol.52 (S1), p.224-224

2018

Volltextzugriff (PDF)

OP09.09: Normal intracranial structure volume analysis between 11 and 20 weeks of gestation by transvaginal 3D neurosonography

Ultrasound in obstetrics & gynecology, 2019-10, Vol.54 (S1), p.114-114

2019

Volltextzugriff (PDF)

OP09.09: Normal intracranial structure volume analysis between 11 and 20weeks of gestation by transvaginal 3D neurosonography

Ultrasound in obstetrics & gynecology, 2019-10, Vol.54 (S1), p.114-114

2019

Volltextzugriff (PDF)

OP 06.06: Low‐set ear in early fetuses with CRL 45‐84mm detected by 3D ultrasound

Ultrasound in obstetrics & gynecology, 2014-09, Vol.44 (S1), p.79-79

2014

Volltextzugriff (PDF)

OP06.06: Low‐set ear in early fetuses with CRL 45‐84mm detected by 3D ultrasound

Ultrasound in obstetrics & gynecology, 2014-09, Vol.44 (S1), p.79-79

2014

Volltextzugriff (PDF)

A Japanese patient with the Costello syndrome

Human genetics, 1994-05, Vol.93 (5), p.605-606

1994

Volltextzugriff (PDF)

Localization of the spherocytosis gene to chromosome segment 8p11.22→8p21.1

Human genetics, 1988, Vol.78 (1), p.94-95

1988

Volltextzugriff (PDF)

Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype

Human molecular genetics, 1994-09, Vol.3 (9), p.1565-1568

1994

Volltextzugriff (PDF)

Electron microscopic study of the differentiation of the digestive tract of the human fetus. (1) Ultrastructure of villi in the human fetus

Nihon Shonika Gakkai zasshi. Acta paediatrica Japonica, 1967-12, Vol.71 (12), p.1498

Chiyo, H

1967

Volltextzugriff (PDF)

Electron microscopic study on the differentiation of the digestive tract of the human fetus. Ultrastructure of pancreatic exocrine cells of the human fetus

Nihon Shonika Gakkai zasshi. Acta paediatrica Japonica, 1967-12, Vol.71 (12), p.1515

Chiyo, H

1967

Volltextzugriff (PDF)

Nonrandom distribution of exchange points in patients with structural rearrangements

American journal of human genetics, 1976-01, Vol.28 (1), p.31-41

1976

Volltextzugriff (PDF)

The oral manifestations of 4p- syndrome

Journal of oral and maxillofacial surgery, 1983-01, Vol.41 (9), p.601-605

1983

Volltextzugriff (PDF)

A case of partial trisomy 3q

Journal of medical genetics, 1976-12, Vol.13 (6), p.525-528

1976

Volltextzugriff (PDF)

Male infant with cat cry syndrome and apparent absence of the Y chromosome

European journal of pediatrics, 1980-05, Vol.133 (3), p.293-296

1980

Volltextzugriff (PDF)

Reciprocal translocation t(5;6)(p13;q27) through three generations: case report of cri du chat syndrome

Human genetics, 1980-02, Vol.53 (2), p.145-147

1980

Volltextzugriff (PDF)

A 6p trisomy detected in a family with a "giant satellite"

Human genetics, 1975-10, Vol.30 (1), p.63-67

1975

Volltextzugriff (PDF)

Possible intrachromosomal duplication in a case of trisomy 9p

Human genetics, 1976-01, Vol.34 (2), p.217-221

1976

Volltextzugriff (PDF)

XXX, XXXXX and XYY syndromes

Nihon rinshō, 1978-05, Vol.Suppl, p.1464

1978

Volltextzugriff (PDF)

Hereditary spherocytic anemia with deletion of the short arm of chromosome 8

American journal of medical genetics, 1995-09, Vol.58 (3), p.225-229

1995

Volltextzugriff (PDF)

The general problem in popularization of human cytogenetic examination (author's transl)

Rinsho byori. The Japanese journal of clinical pathology, 1977-02, Vol.25 (2), p.87

1977

Volltextzugriff (PDF)

1 – 25 von 198

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(167)
Mit Volltextzugriff
(166)

Publikationsform

Artikel
(197)
Tagungsberichte
(1)

Sprache

Englisch
(182)
Japanisch
(27)

Erscheinungsjahr

n.n

Thema

Science & Technology
(126)
Life Sciences & Biomedicine
(106)
Humans
(91)
Male
(57)
Biological And Medical Sciences
(56)
Female
(47)
Medical Sciences
(39)
Animals
(37)
Middle Aged
(24)
Aged
(23)
Adult
(22)
Biochemistry & Molecular Biology
(19)
Fundamental And Applied Biological Sciences. Psychology
(19)
Mice
(17)
Molecular Sequence Data
(16)
Physical Sciences
(15)
Chemistry
(13)
Genetics & Heredity
(12)
Rats
(12)
Adolescent
(11)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Increased Sylvian fissure angle as early sonographic sign of malformation of cortical development

OC18.04: Interhemispheric opening of fetal brain by 3D neurosonography: physiological change and a gourd sign in MCD cases

VP28.06: Which fetuses are indicated for prenatal‐targeted exome sequencing testing? Increased NT or structural anomalies?

P20.01: Low‐set ear detected by three‐dimensional ultrasound in the first trimester and genetic cause

EP08.07: Measurement of Sylvian fissure angles at 18–30 weeks' gestation in cases with neuronal migration disorder

EP08.08: Ventricular occupying ratio at 18–30 weeks' gestation: normal reference range and ventriculomegaly

OP09.09: Normal intracranial structure volume analysis between 11 and 20 weeks of gestation by transvaginal 3D neurosonography

OP09.09: Normal intracranial structure volume analysis between 11 and 20weeks of gestation by transvaginal 3D neurosonography

OP 06.06: Low‐set ear in early fetuses with CRL 45‐84mm detected by 3D ultrasound

OP06.06: Low‐set ear in early fetuses with CRL 45‐84mm detected by 3D ultrasound

A Japanese patient with the Costello syndrome

Localization of the spherocytosis gene to chromosome segment 8p11.22→8p21.1

Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype

Electron microscopic study of the differentiation of the digestive tract of the human fetus. (1) Ultrastructure of villi in the human fetus

Electron microscopic study on the differentiation of the digestive tract of the human fetus. Ultrastructure of pancreatic exocrine cells of the human fetus

Nonrandom distribution of exchange points in patients with structural rearrangements

The oral manifestations of 4p- syndrome

A case of partial trisomy 3q

Male infant with cat cry syndrome and apparent absence of the Y chromosome

Reciprocal translocation t(5;6)(p13;q27) through three generations: case report of cri du chat syndrome

A 6p trisomy detected in a family with a "giant satellite"

Possible intrachromosomal duplication in a case of trisomy 9p

XXX, XXXXX and XYY syndromes

Hereditary spherocytic anemia with deletion of the short arm of chromosome 8

The general problem in popularization of human cytogenetic examination (author's transl)

Suchergebnisse filtern