UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 32

Sortiert nach

Ultrasound detection of eyelashes: a clue for prenatal diagnosis of Cornelia de Lange syndrome

Ultrasound in obstetrics & gynecology, 2013-03, Vol.41 (3), p.341-342

2013

Volltextzugriff (PDF)

Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis

American journal of medical genetics. Part A, 2013-01, Vol.161 (1), p.208-213

2013

Volltextzugriff (PDF)

Artifacts and main lesions in fetal ocular histology

Morphologie, 2023-06, Vol.107 (357), p.207-218

2023

Volltextzugriff (PDF)

Contribution of Diffusion-Weighted Imaging in the Evaluation of Diffuse White Matter Ischemic Lesions in Fetuses: Correlations with Fetopathologic Findings

American journal of neuroradiology : AJNR, 2008-01, Vol.29 (1), p.110-115

2008

Volltextzugriff (PDF)

Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatment

Ultrasound in obstetrics & gynecology, 2022-04, Vol.59 (4), p.513-521

2022

Volltextzugriff (PDF)

L’épaississement des parois artérielles intracrâniennes du système vertebro-basilaire est-il vraiment pathologique ?

Journal of neuroradiology, 2014-03, Vol.41 (1), p.8-8

2014

Volltextzugriff (PDF)

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

Journal of medical genetics, 2011-07, Vol.48 (7), p.497-504

2011

Volltextzugriff (PDF)

Chapitre 94 - Les malformations cérébrales congénitales

Réanimation et soins intensifs en néonatologie, 2016, p.589-597

2016

Volltextzugriff (PDF)

Ultrasound detection of eyelashes: a clue for prenatal diagnosis of Cornelia de Lange syndrome

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 2013, Vol.41 (3), p.341-342

2013

Volltextzugriff (PDF)

Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis

American Journal of Medical Genetics Part A, 2013, Vol.161A (1), p.208-213

2013

Volltextzugriff (PDF)

Finding vacuolated lymphocytes in fetal effusions improves the prenatal diagnosis of lysosomal storage diseases

Prenatal diagnosis, 2020-04, Vol.40 (5), p.605-611

2020

Volltextzugriff (PDF)

Duplicated distal phalanx of thumb or hallux in trisomy 13: A recurrent feature in a series of 42 fetuses

American journal of medical genetics. Part A, 2018-11, Vol.176 (11), p.2325-2330

2018

Volltextzugriff (PDF)

Case report: Antenatal diagnostic of a polymalformative syndrome due to biallelic BRCA2 mutations

Clinical case reports, 2021-09, Vol.9 (9), p.e04838-n/a

2021

Volltextzugriff (PDF)

Inversion duplication deletions involving the long arm of chromosome 13: Phenotypic description of additional three fetuses and genotype-phenotype correlation

American journal of medical genetics. Part A, 2014-10, Vol.164A (10), p.2504-2509

2014

Volltextzugriff (PDF)

Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene

American journal of medical genetics. Part A, 2012-10, Vol.158A (10), p.2430-2438

2012

Volltextzugriff (PDF)

Fetopathologic examination for early termination of pregnancy: dogma or necessity?

American journal of obstetrics and gynecology, 2011-11, Vol.205 (5), p.467.e1-467.e9

2011

Volltextzugriff (PDF)

Abnormal muscle development of the diaphragm in a fetus with 2p14-p16 duplication

American journal of medical genetics. Part A, 2009-12, Vol.149A (12), p.2892-2897

2009

Volltextzugriff (PDF)

Cytomegalovirus-Induced Brain Malformations in Fetuses

Journal of neuropathology and experimental neurology, 2014-02, Vol.73 (2), p.143-158

2014

Volltextzugriff (PDF)

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects

Human molecular genetics, 2014-05, Vol.23 (9), p.2279-2289

2014

Volltextzugriff (PDF)

Inner ear lesions in congenital cytomegalovirus infection of human fetuses

Acta neuropathologica, 2011-12, Vol.122 (6), p.763-774

2011

Volltextzugriff (PDF)

Forensic and pathology remarks concerning the mummified fetuses of King Tutankhamun

American journal of roentgenology (1976), 2012-06, Vol.198 (6), p.W629; author reply W630

2012

Volltextzugriff (PDF)

Growth Restriction, Osteopenia, Placental Massive Perivillous Fibrin Deposition With (or Without) Intervillous Histiocytes and Renal Tubular Dysgenesis—An Emerging Complex

Pediatric and developmental pathology, 2018-01, Vol.21 (1), p.91-94

2018

Volltextzugriff (PDF)

1 – 25 von 32

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(27)
Mit Volltextzugriff
(30)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(23)
Science & Technology
(23)
Humans
(17)
Female
(12)
Genetics & Heredity
(12)
Pregnancy
(9)
Fetuses
(7)
Male
(7)
Biological And Medical Sciences
(6)
Medical Sciences
(6)
Kidneys
(5)
Pathology
(5)
Pediatrics
(5)
Prenatal Diagnosis
(5)
Autopsy
(4)
Life Sciences
(4)
Mutation
(4)
Obstetrics & Gynecology
(4)
Radiology, Nuclear Medicine & Medical Imaging
(4)
Adult
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Ultrasound detection of eyelashes: a clue for prenatal diagnosis of Cornelia de Lange syndrome

Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis

Artifacts and main lesions in fetal ocular histology

Contribution of Diffusion-Weighted Imaging in the Evaluation of Diffuse White Matter Ischemic Lesions in Fetuses: Correlations with Fetopathologic Findings

Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatment

L’épaississement des parois artérielles intracrâniennes du système vertebro-basilaire est-il vraiment pathologique ?

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

Chapitre 94 - Les malformations cérébrales congénitales

Ultrasound detection of eyelashes: a clue for prenatal diagnosis of Cornelia de Lange syndrome

Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis

Finding vacuolated lymphocytes in fetal effusions improves the prenatal diagnosis of lysosomal storage diseases

Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders

Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation

Duplicated distal phalanx of thumb or hallux in trisomy 13: A recurrent feature in a series of 42 fetuses

Case report: Antenatal diagnostic of a polymalformative syndrome due to biallelic BRCA2 mutations

Inversion duplication deletions involving the long arm of chromosome 13: Phenotypic description of additional three fetuses and genotype-phenotype correlation

Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene

Fetopathologic examination for early termination of pregnancy: dogma or necessity?

Abnormal muscle development of the diaphragm in a fetus with 2p14-p16 duplication

Cytomegalovirus-Induced Brain Malformations in Fetuses

Corrigendum to: DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects

Inner ear lesions in congenital cytomegalovirus infection of human fetuses

Forensic and pathology remarks concerning the mummified fetuses of King Tutankhamun

Growth Restriction, Osteopenia, Placental Massive Perivillous Fibrin Deposition With (or Without) Intervillous Histiocytes and Renal Tubular Dysgenesis—An Emerging Complex

Suchergebnisse filtern