Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?

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Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-cn

2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Variable developmental delays ...... 3p22.2 microdeletion syndrome?

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Variable developmental delays ...... 3p22.2 microdeletion syndrome?

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Item

label

Variable developmental delays ...... 3p22.2 microdeletion syndrome?

@en

Variable developmental delays ...... 3p22.2 microdeletion syndrome?

@nl

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Variable developmental delays ...... 3p22.2 microdeletion syndrome?

@en

Variable developmental delays ...... 3p22.2 microdeletion syndrome?

@nl

P1476

Variable developmental delays ...... 3p22.2 microdeletion syndrome?

@en

P2093

Birgitta Bernhard

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Christine M Armour

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Ingrid Cristian

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Jean McGowan-Jordan

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Marc Zucker

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Regina M Zambrano

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Sue Price

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Sunita Venkateswaran

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P2860

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Structure of eIF3b RNA recognition motif and its interaction with eIF3j: structural insights into the recruitment of eIF3b to the 40 S ribosomal subunit

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Identification and characterization of human archaemetzincin-1 and -2, two novel members of a family of metalloproteases widely distributed in Archaea.

Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis.

P304

1593-1600

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P31

scholarly article

P356

10.1002/AJMG.A.38241

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P407

English

P433

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P478

173

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P50

Andrea C Yu

P577

2017-04-25T00:00:00Z

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P698

28440577

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