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Effect of soil and topography on vegetation restoration in an opencast coal mine dump in a loess area

Sheng tai xue bao, 2016, Vol.36 (16)

2016

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

Volltextzugriff (PDF)

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

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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

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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

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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

Volltextzugriff (PDF)

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

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Effect of soil and topography on vegetation restoration in an opencast coal mine dump in a loess area

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

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

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

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

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