(Q33595866)

28 July 2017

title

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype (English)

1 reference

28 July 2017

1 reference

Callen DF

1

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28 July 2017

Eyre H

2

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28 July 2017

Lane S

3

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28 July 2017

Shen Y

4

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28 July 2017

Hansmann I

5

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28 July 2017

Spinner N

6

1 reference

28 July 2017

Zackai E

7

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28 July 2017

McDonald-McGinn D

8

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28 July 2017

Schuffenhauer S

9

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28 July 2017

Wauters J

10

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28 July 2017

language of work or name

English

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publication date

1 October 1993

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

30

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28 July 2017

issue

10

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28 July 2017

page(s)

828-832

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Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Re-evaluation of GM2346 from a del(16)(q22) to t(4;16)(q35;q22.1).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

A view of interphase chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Deletion of 16q with prolonged survival and unusual radiographic manifestations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Reassessment of two apparent deletions of chromosome 16p to an ins(11;16) and a t(1;16) by chromosome painting

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Interstitial deletion of chromosome 16q: 16q22 is critical for 16q- syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

High-resolution cytogenetic-based physical map of human chromosome 16.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016564

Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band region

21 June 2018

1 reference

12 December 2020

16q21 is critical for 16q deletion syndrome

1 reference

12 December 2020

Regional assignment of the human loci for uvomorulin (UVO) and chymotrypsinogen B (CTRB) with the help of two overlapping deletions on the long arm of chromosome 16

1 reference

12 December 2020

Interstitial deletion of 16(q13q22) in a newborn resulting from a paternal insertional translocation

1 reference

12 December 2020

Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46,XX,del(16))q21)

1 reference

12 December 2020

A terminal long arm deletion of chromosome 16 in a dysmorphic infant: 46,XY,del(16) (q22)

1 reference

12 December 2020

1 reference

12 December 2020

The chromosome constitution of 1000 human spermatozoa

1 reference

12 December 2020

Interstitial deletion for a region in the long arm of chromosome 16

1 reference

12 December 2020

Deletion of band 13q21 is compatible with normal phenotype

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.30.10.828

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28 July 2017

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28 July 2017

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