UB Paderborn / Katalog / Suche / in CDI

1 – 16 von 16

Sortiert nach

Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Zhonghua yi xue yi chuan xue za zhi, 2023-08, Vol.40 (8), p.966

2023

Link zum Volltext

Verfügbarkeit prüfen

Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation

Zhonghua yi xue yi chuan xue za zhi, 2023-02, Vol.40 (2), p.230

2023

Link zum Volltext

Verfügbarkeit prüfen

Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate

Zhonghua yi xue yi chuan xue za zhi, 2021-01, Vol.38 (1), p.52

2021

Link zum Volltext

Verfügbarkeit prüfen

Genetic analysis of 90 families affected with spinal muscular atrophy

Zhonghua yi xue yi chuan xue za zhi, 2020-02, Vol.37 (2), p.116

2020

Link zum Volltext

Verfügbarkeit prüfen

Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

Zhonghua yi xue yi chuan xue za zhi, 2020-01, Vol.37 (1), p.17

2020

Link zum Volltext

Verfügbarkeit prüfen

Genetic analysis of a pedigree affected with distal hereditary motor neuronopathy V

Zhonghua yi xue yi chuan xue za zhi, 2019-03, Vol.36 (3), p.207

2019

Link zum Volltext

Verfügbarkeit prüfen

Analysis of genetic polymorphisms and mutations of 20 frequently used STR loci among ethnic Hans from Henan

Zhonghua yi xue yi chuan xue za zhi, 2017-04, Vol.34 (2), p.266

2017

Link zum Volltext

Verfügbarkeit prüfen

Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia

Zhonghua yi xue yi chuan xue za zhi, 2016-10, Vol.33 (5), p.629

2016

Link zum Volltext

Verfügbarkeit prüfen

Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 14q deletion

Zhonghua yi xue yi chuan xue za zhi, 2016-06, Vol.33 (3), p.361

2016

Link zum Volltext

Verfügbarkeit prüfen

Phenotypic and genetic analysis of a boy with partial trisomy of 1q

Zhonghua yi xue yi chuan xue za zhi, 2017-06, Vol.34 (3), p.398

2017

Link zum Volltext

Verfügbarkeit prüfen

Association of MTHFR and MTRR genes polymorphisms with non-disjunctions of chromosomes 18 and 21

Zhonghua yi xue yi chuan xue za zhi, 2015-06, Vol.32 (3), p.395

2015

Link zum Volltext

Verfügbarkeit prüfen

Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome

Zhonghua yi xue yi chuan xue za zhi, 2015-12, Vol.32 (6), p.823

2015

Link zum Volltext

Verfügbarkeit prüfen

Genetic diagnosis for a family without exonic deletions and duplications of dystrophin gene

Zhonghua yi xue yi chuan xue za zhi, 2015-02, Vol.32 (1), p.81

2015

Link zum Volltext

Verfügbarkeit prüfen

Progress of research on the pathogenesis of obesity in Bardet-Biedl syndrome

Zhonghua yi xue yi chuan xue za zhi, 2016-12, Vol.33 (6), p.871

2016

Link zum Volltext

Verfügbarkeit prüfen

Controlled growth of mesoporous ZnCoO nanosheet arrays on Ni foam as high-rate electrodes for supercapacitors

RSC advances, 2014-10, Vol.4 (5), p.2393-2397

2014

Link zum Volltext

Verfügbarkeit prüfen

Analysis of the effect of noninvasive positive-pressure ventilation with simultaneous detection of Dx-pH monitoring in oropharynx and esophagus for 48 hours in patients with moderate and severe OSA

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery, 2020-12, Vol.34 (12), p.1083

2020

Link zum Volltext

Verfügbarkeit prüfen

1 – 16 von 16

Suche als RSS-Feed

Aktive Filter

SpracheEnglisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1)
Mit Volltextzugriff
(1)

Publikationsform

Artikel
(16)

Sprache

Chinesisch
(15)

Erscheinungsjahr

n.n

Thema

Humans
(15)
Female
(10)
Pedigree
(6)
Child, Preschool
(5)
Male
(4)
Mutation
(4)
Phenotype
(4)
Prenatal Diagnosis
(4)
Array Comparative Genomic Hybridization
(3)
Asian Continental Ancestry Group - Genetics
(3)
China
(3)
Mental Retardation
(3)
Microsatellite Repeats
(3)
Pregnancy
(3)
Abnormalities, Multiple - Genetics
(2)
Adolescent
(2)
Adult
(2)
Asian Continental Ancestry Group - Ethnology
(2)
Child
(2)
Chromosome Banding
(2)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

Zeitschrift / Serie

Menü

Weitere Dienste

Einstellungen

Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation

Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate

Genetic analysis of 90 families affected with spinal muscular atrophy

Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

Genetic analysis of a pedigree affected with distal hereditary motor neuronopathy V

Analysis of genetic polymorphisms and mutations of 20 frequently used STR loci among ethnic Hans from Henan

Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia

Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 14q deletion

Phenotypic and genetic analysis of a boy with partial trisomy of 1q

Association of MTHFR and MTRR genes polymorphisms with non-disjunctions of chromosomes 18 and 21

Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome

Genetic diagnosis for a family without exonic deletions and duplications of dystrophin gene

Progress of research on the pathogenesis of obesity in Bardet-Biedl syndrome

Controlled growth of mesoporous ZnCoO nanosheet arrays on Ni foam as high-rate electrodes for supercapacitors

Analysis of the effect of noninvasive positive-pressure ventilation with simultaneous detection of Dx-pH monitoring in oropharynx and esophagus for 48 hours in patients with moderate and severe OSA

Aktive Filter

Suchergebnisse filtern