Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

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Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

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Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

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Item

label

Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

@en

Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

@nl

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Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

@en

Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

@nl

P1476

Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

@en

P2093

Anju Shukla

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Siddaramappa J Patil

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Yougal Kishore

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P2860

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.

The 22q11 deletion syndromes.

Endocrine aspects of the 22q11.2 deletion syndrome.

New height, weight and head circumference charts for British children with Williams syndrome.

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome.

Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.

Clinical features and follow-up in patients with 22q11.2 deletion syndrome.

Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.

Clinical features of 78 adults with 22q11 Deletion Syndrome.

P304

1927-1931

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scholarly article

P356

10.1002/AJMG.A.37116

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P407

English

P433

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P478

167A

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P50

Kausik Mandal

Katta Mohan Girisha

Shubha R Phadke

P577

2015-04-21T00:00:00Z

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P698

25898978

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