POGZ-CHAMP1 ARE MOLECULAR PARTNERS ASSOCIATED WITH NEURODEVELOPMENTAL DISORDERS AND PHENOTYPIC ONTOLOGY FOR OLFACTORY BULB HYPOPLASIA AND INTESTINAL MALROTATION

Shieh J. T.; Abadie J. M.

首页> 外文期刊>American journal of medical genetics, Part A >POGZ-CHAMP1 ARE MOLECULAR PARTNERS ASSOCIATED WITH NEURODEVELOPMENTAL DISORDERS AND PHENOTYPIC ONTOLOGY FOR OLFACTORY BULB HYPOPLASIA AND INTESTINAL MALROTATION

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POGZ-CHAMP1 ARE MOLECULAR PARTNERS ASSOCIATED WITH NEURODEVELOPMENTAL DISORDERS AND PHENOTYPIC ONTOLOGY FOR OLFACTORY BULB HYPOPLASIA AND INTESTINAL MALROTATION

机译：Pogz-Champ1是与神经发育疾病和表型患有嗅球发育不全的表型本体相关的分子伴侣和肠道恶性肿瘤

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来源
《American journal of medical genetics, Part A》 |2019年第4期|共1页
作者
Shieh J. T.; Abadie J. M.;
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作者单位

Univ Calif San Francisco Med Genet Inst Human Genet San Francisco CA 94143 USA;

Univ Calif San Francisco Med Genet Inst Human Genet San Francisco CA 94143 USA;

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原文格式 PDF
正文语种 eng
中图分类医学遗传学;
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入库时间 2022-08-20 02:16:07

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1. POGZ-CHAMP1 ARE MOLECULAR PARTNERS ASSOCIATED WITH NEURODEVELOPMENTAL DISORDERS AND PHENOTYPIC ONTOLOGY FOR OLFACTORY BULB HYPOPLASIA AND INTESTINAL MALROTATION [J] . Shieh J. T., Abadie J. M. American journal of medical genetics, Part A . 2019,第4期

机译：Pogz-Champ1是与神经发育疾病和表型患有嗅球发育不全的表型本体相关的分子伴侣和肠道恶性肿瘤
2. Phenotypic and Molecular Convergence of 2q23.1 Deletion Syndrome with Other Neurodevelopmental Syndromes Associated with Autism Spectrum Disorder [J] . Joseph T. Alaimo, Li Chen, Merlin G. Butler, International Journal of Molecular Sciences . 2015,第4期

机译：2q23.1缺失综合征与其他与自闭症谱系障碍相关的神经发育综合征的表型和分子融合
3. Pituitary stalk interruption and olfactory bulbs aplasia/hypoplasia in a man with Kallmann syndrome and reversible gonadotrope and somatotrope deficiencies [J] . Sarfati Julie, Saveanu Alexandru, Young Jacques Endocrine. . 2015,第3期

机译：患有Kallmann综合征和可逆性性腺症和体质缺乏症的男性的垂体柄中断和嗅球发育不良/发育不全
4. Molecular regulation of postnatal neurogenesis in the mammalian subventricular zone-olfactory bulb pathway. [D] . Wang, Tsu-Wei. 2006

机译：哺乳动物脑室下带嗅球途径中产后神经发生的分子调控。
5. Olfactory bulb hypoplasia in Prokr2 null mice stems from defective neuronal progenitor migration and differentiation [O] . Haydn M Prosser, Allan Bradley, Maeve A Caldwell -1

机译：Prokr2缺失小鼠的嗅球发育不全源自神经元祖细胞的迁移和分化缺陷
6. EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum [O] . Ulrike Hüffmeier, Cornelia Kraus, Miriam S. Reuter, 2021

机译：EIF3F相关的神经发育障碍：精制表型和扩展分子谱

POGZ-CHAMP1 ARE MOLECULAR PARTNERS ASSOCIATED WITH NEURODEVELOPMENTAL DISORDERS AND PHENOTYPIC ONTOLOGY FOR OLFACTORY BULB HYPOPLASIA AND INTESTINAL MALROTATION

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