(Q33588304)

28 July 2017

title

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

1 reference

28 July 2017

Roberts SH

1

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28 July 2017

Duckett DP

series ordinal

2

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28 July 2017

language of work or name

English

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publication date

1 October 1978

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

15

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28 July 2017

issue

5

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28 July 2017

page(s)

375-381

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Metaphyseal dysostosis. Review of literature; study of a case with cytogenetic analysis

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=1013735

Chromosome preparations of leukocytes cultured from human peripheral blood

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Trisomy-16 in a mosaic carrier father and his aborted foetus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Chromosome abnormalities in early spontaneous abortions

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Trisomy of chromosome 16 in a neonate, 47XY,?16+

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Chromosome constitution of 500 infants dying during the perinatal period. With an appendix concerning other genetic disorders among these infants

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Banding analysis of abnormal karyotypes in spontaneous abortion

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Chromosome studies in investigation of stillbirths and neonatal deaths

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Anti-mongolism. Studies in an infant with a partial monosomy of the 21 chromosome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

An abortus with a normal/trisomy 16 mosaicism: instability of trisomic cells in vitro

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Tertiary trisomy, 47,XX,+14q--, resulting from maternal balanced translocation, 46,XX,t(14;16)(q11;q24)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced state

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

New Chromosomal Syndromes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

CHROMOSOME STUDIES ON SPONTANEOUS ABORTIONS

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013735

[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME.]

31 October 2018

1 reference

12 December 2020

TRISOMY OF AUTOSOME 16

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

Chromosome anomalies as a cause of spontaneous abortion

1 reference

12 December 2020

Effect of gestational and maternal age in early abortion

1 reference

12 December 2020

Group E triple cell line mosaicism with Sprengel's deformity and other asymmetrical congenital abnormalities. Report of a case

1 reference

12 December 2020

A cytogenetic study of human spontaneous abortions using banding techniques

1 reference

12 December 2020

Recent advances in the cytogenetic study of human spontaneous abortions

1 reference

12 December 2020

Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome

1 reference

12 December 2020

A balanced translocation (3p+; 16q-) in a mother as the most probable cause of multiple stillborn or premature born infants (author's transl)

1 reference

12 December 2020

Balanced translocation t(15q-;16p+) as cause of habitual abortions

1 reference

12 December 2020

Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms

1 reference

12 December 2020

16q trisomy in a family with a balanced 15/16 translocation

1 reference

12 December 2020

Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1

1 reference

12 December 2020

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

1 reference

12 December 2020

Clinical and cytogenetic aspects of the 21 deletion syndrome

1 reference

12 December 2020

A ring chromosome No. 16 in an infant with primary hypoparathyroidism

1 reference

12 December 2020

The G deletion syndromes

1 reference

12 December 2020

Identifiers

PMC publication ID

1013735

1 reference

28 July 2017

1 reference