Gao M - Search Results

1

Genotypic and phenotypic characteristics of 12 chinese children with glycogen storage diseases.

Dong R, Wei X, Zhang K, Song F, Lv Y, Gao M, Wang D, Ma J, Gai Z, Liu Y. Dong R, et al. Among authors: gao m. Front Genet. 2022 Aug 29;13:932760. doi: 10.3389/fgene.2022.932760. eCollection 2022. Front Genet. 2022. PMID: 36105079 Free PMC article.

2

[Diagnosis of a case with oculocutaneous albinism type Ⅲ with next generation exome capture sequencing].

Lyu Y, Huang J, Zhang K, Liu G, Gao M, Gai Z, Liu Y. Lyu Y, et al. Among authors: gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Feb 10;34(1):73-77. doi: 10.3760/cma.j.issn.1003-9406.2017.01.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28186599 Chinese.

3

[Analysis of genetic etiology of a female with 47,XXY syndrome].

Li H, Zhang K, Gao M, Zhang H, Wang Y, Zhang Y, Liu Y, Gai Z. Li H, et al. Among authors: gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Feb 10;34(1):102-105. doi: 10.3760/cma.j.issn.1003-9406.2017.01.024. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28186606 Chinese.

4

Novel OFD1 frameshift mutation in a Chinese boy with Joubert syndrome: a case report and literature review.

Zhang K, Meng C, Ma J, Gao M, Lv Y, Liu Y, Gai Z. Zhang K, et al. Among authors: gao m. Clin Dysmorphol. 2017 Jul;26(3):135-141. doi: 10.1097/MCD.0000000000000183. Clin Dysmorphol. 2017. PMID: 28505061 Review.

5

Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking.

Liu S, Zhang K, Song F, Yang Y, Lv Y, Gao M, Liu Y, Gai Z. Liu S, et al. Among authors: gao m. Cytogenet Genome Res. 2017;152(1):1-8. doi: 10.1159/000477520. Epub 2017 Jun 24. Cytogenet Genome Res. 2017. PMID: 28647735

6

[Genetic analysis of two pediatric patients with Beckwith-Wiedemann syndrome].

Li X, Lyu Y, Gao M, Yan X, Meng C, Zhang K, Liu Y, Gai Z. Li X, et al. Among authors: gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):831-834. doi: 10.3760/cma.j.issn.1003-9406.2017.06.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188610 Chinese.

7

Clinical characteristics and mutation analysis of five Chinese patients with maple syrup urine disease.

Li X, Yang Y, Gao Q, Gao M, Lv Y, Dong R, Liu Y, Zhang K, Gai Z. Li X, et al. Among authors: gao m, gao q. Metab Brain Dis. 2018 Jun;33(3):741-751. doi: 10.1007/s11011-017-0168-0. Epub 2018 Jan 6. Metab Brain Dis. 2018. PMID: 29307017

8

[Analysis of SLC25A13 gene mutations in five infants with neonatal intrahepatic cholestasis caused by citrin deficiency].

Xu J, Gao M, Lyu Y, Tang Y, Wei X, Yang L, Zhang K, Liu Y, Gai Z. Xu J, et al. Among authors: gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Feb 10;35(1):34-38. doi: 10.3760/cma.j.issn.1003-9406.2018.01.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29419856 Chinese.

9

[Diagnose of a neonate with X-linked thrombocytopenia by next generation sequencing].

Gao M, Kang L, Liu Y, Gai Z. Gao M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):422-425. doi: 10.3760/cma.j.issn.1003-9406.2018.03.026. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896746 Chinese.

10

[Analysis of a neonate with bullous congenital ichthyosiform erythroderma with next generation sequencing].

Lyu Y, Shi C, Zhang K, Gao M, Liu Y. Lyu Y, et al. Among authors: gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):434-436. doi: 10.3760/cma.j.issn.1003-9406.2018.03.029. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896749 Chinese.

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