(Q40020590)

English

The syndrome associated with the partial D-monosomy. Case report and review

scientific article published on January 1971

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

The syndrome associated with the partial D-monosomy. Case report and review (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

author name string

D J Orbeli

1

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

I W Lurie

2

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

J L Goroshenko

3

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 January 1971

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

13

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

296-308

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

Multiple congenital anomalies associated with a ring-D chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinoblastoma and deletion D (14) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A ring D chromosome and anomalous inheritance of haptoglobin type

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A malformation syndrome with ring D chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative behavior of ring chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Karyotype and phenotype of autosome aberrations in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ABNORMALITIES WITH RING CHROMOSOME

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring Chromosome D (13)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absent thumbs with a ring D2 chromosome: a new deletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Ocular abnormalities of phenotype DR (ring D chromosome)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring Chromosomes in Human Beings

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of D ring chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the duplication of circular structures

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A human ring D chromosome associated with multiple congenital abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring chromosomes in two infants with congenital malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Symptomatology of the ring chromosomes of the D group. (2 new observations of type 13r)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Dr phenotype: a study of threee cases with a ring D chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple congenital abnormalities associated with ring chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 13q-deletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant serum protein inheritance in a patient with a ring D chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral colobomas of iris and choroid. Association with partial deletion of a chromosome of group D

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dq-, multiple malformations and retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple abnormalities in a newborn infant with a D1ring chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complex chromosomic mosaic: trisomy D, partial disomy in large telocentrism

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial deletion of the long arm of a group D (13-15) chromosome :Dq-

1 reference

https://pubmed.ncbi.nlm.nih.gov/5135849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

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