Forty four probands with an additional "marker" chromosome. (Q52090526)

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scientific article published in January 1985

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English	Forty four probands with an additional "marker" chromosome.	scientific article published in January 1985

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scholarly article

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Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

title

Forty four probands with an additional "marker" chromosome. (English)

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Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

author name string

K E Buckton

series ordinal

1

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Europe PubMed Central

PubMed publication ID

3857214

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22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

G Spowart

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2

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Europe PubMed Central

PubMed publication ID

3857214

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22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

M S Newton

series ordinal

3

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Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

H J Evans

series ordinal

4

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Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

publication date

1 January 1985

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Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

published in

Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

volume

69

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stated in

Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

page(s)

353-370

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Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

cites work

Supernumerary chromosomes in six patients

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

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inferred from PubMed ID database lookup

An extra idic(15p)(q11) chromosome in Prader-Willi syndrome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further studies on the frequency of constitutional chromosome abnormalities in patients with malignant disease

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cat-eye syndrome, a partial trisomy 22

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

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The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

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New technique for distinguishing between human chromosomes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

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inferred from PubMed ID database lookup

Chromosome surveys in penal institutions and approved schools

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

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Leukocytes Cultured from Small Inocula of Whole Blood and the Preparation of Metaphase Chromosomes by Treatment with Hypotonic KCL

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

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A small supernumerary metacentric chromosome: interprétation test (author's transl)

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two kinships with accessory bisatellited chromosomes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autoradiographic investigations of centric fragments and rings in patients with stigmata of gonadal dysgenesis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic and clinical studies in five cases of inv dup(15)

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome and a bisatellited derivative of chromosome 15

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cat-eye syndrome with unusual marker chromosome probably not chromosome 22

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital hypothyroidism in Klinefelter's syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

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inferred from PubMed ID database lookup

Heteromorphic X chromosomes in 46,XX males: Evidence for the involvement of X-Y interchange

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic significance of accessory bisatellited marker chromosomes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Small accessory chromosomes (SAC) and their genotype--phenotype correlation

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An extra small metacentric chromosome identified as a deleted chromosome No. 17

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of a small metacentric chromosome: Familial and cytogenetic evidence

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

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[Trisomy 21 by translocation (21q,21q) in two sibs of a mother with a supernumerary microchromosome (author's transl)]

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

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inferred from PubMed ID database lookup

B-Chromosome Systems in Flowering Plants and Animal Species

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential maternal derivation in inv dup(15): analysis of eight new cases.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome changes in Alzheimer's presenile dementia

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The aetiology of the cat eye syndrome reconsidered

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple technique for demonstrating centromeric heterochromatin

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytogenetic survey of 11,680 newborn infants

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/3857214

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C-bands in seven cases of accessory small chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome survey of new patients admitted to the four maximum security hospitals in the United Kingdom

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significance of detection of extra metacentric microchromosome in amniotic cell culture

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Properties and significance of a small marker chromosome in amniotic fluid cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A G-band study of chromosomes in liveborn infants

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome abnormalities in human embryos after in vitro fertilization

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The origin and behavior of two isodicentric bisatellited chromosomes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytogenetic study of 1000 spontaneous abortions

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

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Cytogenetics and infertility in man. I. Karyotype and seminal analysis: results of a five-year survey of men attending a subfertility clinic

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome studies on male patients at a mental subnormality hospital

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal detection of an accessory chromosome identified as an inversion duplication (15)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inv dup (15) with mental retardation but few dysmorphic features

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3857214

retrieved

12 December 2020

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Identifiers

DOI

10.1007/BF00291656

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Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

Fatcat ID

release_agxaedzzkzdehjnp5pvd5ip6ay

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24 November 2022

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PubMed publication ID

3857214

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3857214

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/3857214

 

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