(Q33595243)

28 July 2017

title

Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features (English)

1 reference

28 July 2017

Trautmann U

1

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28 July 2017

Pfeiffer RA

series ordinal

2

1 reference

28 July 2017

Seufert-Satomi U

series ordinal

3

1 reference

28 July 2017

Tietze HU

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 April 1993

1 reference

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

4

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28 July 2017

page(s)

330-331

1 reference

Deletion of 16q with prolonged survival and unusual radiographic manifestations

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=1016348

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=1016348

Duplication of distal 19q: clinical report and review

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016348

Variation in the centromeric banding of chromosome 19*

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016348

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016348

G-banding patterns of high-resolution human chromosomes 6?22, X, and Y

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016348

Trisomy for the distal third of the long arm of chromosome 19 in brother and sister

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016348

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

21 June 2018

1 reference

12 December 2020

Centromere heteromorphism in chromosome 19

1 reference

12 December 2020

16q21 is critical for 16q deletion syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.30.4.330

1 reference

28 July 2017

1 reference

28 July 2017

1 reference