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NA06097 DNA from Fibroblast

Description:

MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS

Affected:

Yes

Sex:

Female

Age:

1 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Chromosome Abnormalities
dbGaP
Class Disorders of the Nervous System
Quantity 10 µg
Quantitation Method Please see our FAQ
Biopsy Source Arm
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source DNA from Fibroblast
Race White
Family Member 1
Relation to Proband proband
Confirmation Karyotypic analysis and Case history
ISCN 46,XX,del(17)(:p13->qter).ish del(17)(pter->p13.3::p13.1->qter)(VIJy2185-,17ptel180+,LISI-,FLI+,17qtel13+)
Species Homo sapiens
Common Name Human
Remarks Clinically affected; typical facies (bitemporal hollowing, thin downturned upper lip, micrognathia, microcephaly, high arched palate); ventricular septal defect; cell line initially noted additional diagnosis of a translocated chromosome, as it was submitted with the following karyotype: 46,XX,-17,+der(17),t(7;17)(p22.3;p13.2)pat; upon further analysis of several passages with advanced cytogenomic techniques, it was confirmed the translocation was not present in the cell line and this diagnosis has been subsequently removed.

Characterizations

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PDL at Freeze 6
Passage Frozen 6
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Chromosome Analysis
 
Cytogenetics Chromosome 17: DELETION Aneuploid Segment (-).ish del(17)(pter->p13.3::p13.1->qter)
Chromosome 17: DERIVATIVE CHROMOSOME Aneuploid Segment (-)17pter>17p13
Chromosome 7: DERIVATIVE CHROMOSOME Aneuploid Segment (+)7pter>7p22
Chromosome 7: DERIVATIVE CHROMOSOME Trisomic Segment 7pter>7p22

Phenotypic Data

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Remarks Clinically affected; typical facies (bitemporal hollowing, thin downturned upper lip, micrognathia, microcephaly, high arched palate); ventricular septal defect; cell line initially noted additional diagnosis of a translocated chromosome, as it was submitted with the following karyotype: 46,XX,-17,+der(17),t(7;17)(p22.3;p13.2)pat; upon further analysis of several passages with advanced cytogenomic techniques, it was confirmed the translocation was not present in the cell line and this diagnosis has been subsequently removed.

Publications

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Goh CJ, Kwon HJ, Kim Y, Jung S, Park J, Lee IK, Park BR, Kim MJ, Kim MJ, Lee MS, Improving CNV Detection Performance in Microarray Data Using a Machine Learning-Based Approach Diagnostics (Basel, Switzerland)14: 2023
PubMed ID: 38201393
 
Mahendran G, Breger K, McCown PJ, Hulewicz JP, Bhandari T, Addepalli B, Brown JA, Multi-Omics Approach Reveals Genes and Pathways Affected in Miller-Dieker Syndrome Molecular neurobiology14: 2023
PubMed ID: 39508990
 
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013
PubMed ID: 23665875

External Links

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dbSNP dbSNP ID: 18751
Gene Cards MDCR
NCBI Gene Gene ID:4186
NCBI GTR 247200 MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS
OMIM 247200 MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS
Omim Description MDSMILLER-DIEKER SYNDROME CHROMOSOME REGION, INCLUDED; MDCR, INCLUDED
  MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS

Images

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View copy number variation 
copy number variation 
Pricing
International/Commercial/For-profit:
$281.00USD
U.S. Academic/Non-profit/Government:
$139.00USD
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How to Order
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