Partial Deletion of Chromosome 1p31.1 Including only the Neuronal Growth Regulator 1 Gene in Two Siblings

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Glycosylphosphatidylinositol-Anchored Immunoglobulin Superfamily Cell Adhesion Molecules and Their Role in Neuronal Development and Synapse Regulation.Neuronal Growth and Behavioral Alterations in Mice Deficient for the Psychiatric Disease-Associated Negr1 Gene.

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Q47910942-C31D9B53-2DC6-4AFF-B6D6-B7681516B649 Q50421930-54E03F0B-DBB8-4419-AA34-0134824FB825

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Partial Deletion of Chromosome 1p31.1 Including only the Neuronal Growth Regulator 1 Gene in Two Siblings

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on March 2015

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Partial Deletion of Chromosome ...... gulator 1 Gene in Two Siblings

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Partial Deletion of Chromosome ...... ulator 1 Gene in Two Siblings.

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Partial Deletion of Chromosome ...... gulator 1 Gene in Two Siblings

@en

Partial Deletion of Chromosome ...... ulator 1 Gene in Two Siblings.

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Partial Deletion of Chromosome ...... gulator 1 Gene in Two Siblings

@en

Partial Deletion of Chromosome ...... ulator 1 Gene in Two Siblings.

@nl

P1476

Partial Deletion of Chromosome ...... gulator 1 Gene in Two Siblings

@en

P2093

Merlin G Butler

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Ensembl 2014

Functional inactivation of the genome-wide association study obesity gene neuronal growth regulator 1 in mice causes a body mass phenotype

Characterization of a novel rat brain glycosylphosphatidylinositol-anchored protein (Kilon), a member of the IgLON cell adhesion molecule family

De novo interstitial deletion del(1)(p21p32).

Interstitial deletion 1p in a 30 year old woman.

Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.

A homozygous 237-kb deletion at 1p31 identified as the locus for midline cleft of the upper and lower lip in a consanguineous family

Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia

Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity.

Two cases of interstitial deletion 1p

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23-28

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scholarly article

case report

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10.1055/S-0035-1554977

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Devin M Cox

Ann Genovese

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2015-03-01T00:00:00Z

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P698

27617112

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sibling

P932

4906414

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Partial Deletion of Chromosome 1p31.1 Including only the Neuronal Growth Regulator 1 Gene in Two Siblings

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P2860

P2860

Partial Deletion of Chromosome 1p31.1 Including only the Neuronal Growth Regulator 1 Gene in Two Siblings

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932