Interchromosomal insertions. Identification of five cases and a review.

Interchromosomal insertions. Identification of five cases and a review.

Item
http://www.wikidata.org/entity/Q34120339
Male and female meiotic behaviour of an intrachromosomal insertion determined by preimplantation genetic diagnosis.A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridizationRecurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH.X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies.Chromosomal Abnormalities in Infertile Men from Southern India.Mechanisms for Complex Chromosomal Insertions.Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients.Detecting rearrangements in children using subtelomeric FISH and SKY.Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).Interstitial Chromosome 3p14.1 Deletion due to a Maternal Insertion: Phenotype and Association with Balanced Parental Rearrangement.An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4.Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings.Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results.Balanced complex chromosome rearrangements: reproductive aspects. A review.Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder.Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques
P2860

Interchromosomal insertions. Identification of five cases and a review.

Item
http://www.wikidata.org/entity/Q34120339
description
2000 nî lūn-bûn
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2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Interchromosomal insertions. Identification of five cases and a review.
@ast
Interchromosomal insertions. Identification of five cases and a review.
@en
Interchromosomal insertions. Identification of five cases and a review.
@nl
type
label
Interchromosomal insertions. Identification of five cases and a review.
@ast
Interchromosomal insertions. Identification of five cases and a review.
@en
Interchromosomal insertions. Identification of five cases and a review.
@nl
prefLabel
Interchromosomal insertions. Identification of five cases and a review.
@ast
Interchromosomal insertions. Identification of five cases and a review.
@en
Interchromosomal insertions. Identification of five cases and a review.
@nl
P1433
P1476
P2093
P2888
P304
P31
P356
P433
P478
P577
P6179
P698
P356
P1433
P1476
Interchromosomal insertions. Identification of five cases and a review.
@en
P2093
P2888
P304
P31
P356
P433
P478
P577
P6179
P698