2q13

A transmitted deletion of 2q13 to 2q141 causes no phenotypic

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of phenotypic observations in 2q13 deletion and duplication carriers

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PCR detected the chromosome 2q13 deletion in patient 1 her mother and

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2q13 microdeletion syndrome Report on a newborn with additional

Minimum common region of homozygous loss at 2q13 and expression of BIM

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Recurrent deletions and duplications of chromosome 2q112 and 2q13 are

A schematic comparison of the chromosome 2q13 deletions identified in

Mikrodeletion 2Q13 Mikrodelektion und Mikroduplikationssyndrome CKXA

ITS at 22q112 and 2q13 detected by doublestrand PRINS with telomeric

A recurrent 2q13 microdeletion involving TMEM87B Graphical

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A transmitted deletion of 2q13 to 2q141 causes no phenotypic

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Screening of candidate genes within the 2q13 CR by antisense morpholino

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A new case of 2q duplication supports either a locus for orofacial

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Figure 1 from Gene content and function of the ancestral chromosome

Figure 1 from A New Case of 13q122q131 Microdeletion Syndrome

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Structurally divergent and recurrently mutated regions of primate

Discovery of a potentially deleterious variant in TMEM87B in a patient

Absence of aneuploidy and gastrointestinal tumours in a man with a

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Figure 1 from A New Case of 13q122q131 Microdeletion Syndrome

22q133 deletion syndrome MedlinePlus Genetics

Microdeletionduplication at 15q132q133 among individuals with

Experimental and Therapeutic Medicine

De novo deletion 14q112q13 including PAX9 clinical and molecular

Table 1 from Monozygotic Dichorionic Twins Heterokaryotypic for

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Unilateral Opercular Polymicrogyria in a Girl with 22q13 Deletion Syndrome

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Microdeletions in the 15q112q132 region identified in patients 1 and

15q11.2q13区域缺失重复综合征（15q11.2缺失综合征、小胖威廉综合征、天使综合征）疾病介绍及应对策略 - 知乎

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Identification of a novel locus on chromosome 2q13 which predisposes

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The complex behavioral phenotype of 15q133 microdeletion syndrome

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The Variant inv2p112q13 Is a Genuinely Recurrent Rearrangement but

The Interstitial Duplication 15q112q13 Syndrome Includes Autism Mild

Absence of aneuploidy and gastrointestinal tumours in a man with a

22q133 deletion syndrome MedlinePlus Genetics

PraderWilli syndrome 46XYdel15q112q131 Reference Standard

Cytogenetic and molecular analysis of the 20q132q133 deletion from

Schematic representation showing deletions in the 22q1331 chromosome

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Epilepsy with myoclonic absence presenting with unilateral jerks A

22q133 deletion syndrome MedlinePlus Genetics

BCL2L11を含む2q13欠失症候群 - マイクロアレイ染色体検査の診断・診療体制の構築｜東京女子医科大学ゲノム診療科

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Cytogenetic and molecular analysis of the 20q132q133 deletion from

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Chromosomal microarray analysis detects a 18 Mbduplication of the

15q11q13 duplication syndrome MedlinePlus Genetics

Microdeletionduplication at 15q132q133 among individuals with

A report on seven fetal cases associated with 15q11q13 microdeletion

A child with mosaicism for deletion 14q112q13 PMC

Human Chromosome 2 Fusion in Hominin Evolution Cytogenetic Evidence

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Further delineation of the 15q13 microdeletion and duplication

Discovery of a potentially deleterious variant in TMEM87B in a patient

A child with mosaicism for deletion 14q112q13 PMC

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Olfactory ReceptorRelated Duplicons Mediate a Microdeletion at 11q13

Main characteristics of 22q13 deletion cases presented in this study

Whole genome sequencing identifies a duplicated region encompassing

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15Q133 Microduplication Syndrome ZMIF

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Identification of a novel locus on chromosome 2q13 which predisposes

A novel microdeletion syndrome at 3q1331 characterised by

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22q13

The Variant inv2p112q13 Is a Genuinely Recurrent Rearrangement but

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Four novel NAHRprone regions on chromosome 2q122q13 Top Schematic

Microdeletions in the 15q112q132 region identified in patients 1 and

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