(Q35231124)

7 August 2017

Frequency and occurrence of chromosomal syndromes: II. E-trisomy (English)

1 reference

7 August 2017

Conen PE

1

1 reference

PubMed ID

17948514

7 August 2017

Erkman B

series ordinal

2

1 reference

PubMed ID

17948514

7 August 2017

language of work or name

English

0 references

publication date

1 July 1966

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

18

1 reference

7 August 2017

4

1 reference

7 August 2017

387-398

1 reference

Incidence of mongolism and its diagnosis in the newborn.

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

Incidence, Mortality, and Sex Distribution of Mongoloid Defectives

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

CHROMOSOME 18: A TOPOLOGIC APPROACH.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

17-18 TRISOMY SYNDROME; REVIEW AND REPORT OF A CASE.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

The relationship between congenital anomalies and autosomal chromosome abnormalities

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

Trisomy-17 syndrome. Report of three cases and review of the literature

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

13 July 2018

A new trisomic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

Frequency and occurrence of chromosomal syndromes. I. D-Trisomy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

The epidemiology of chromosome aberrations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

Autoimmunity and chromosomal aberrations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

13 July 2018

Amitriptyline poisoning.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

GENETIC PROGNOSIS AND COUNSELING.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

MULTIPLE CONGENITAL ANOMALIES IN THE E1-TRISOMY (GROUP 16-18) SYNDROME

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

TRISOMY-18 SYNDROME: CASE REPORT WITH CHROMOSOMAL ANALYSIS

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706095

A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome

26 September 2018

1 reference

12 December 2020

THE TRISOMY-18 SYNDROME. REPORT ON 3 CASES

1 reference

12 December 2020

THE TRISOMY 18 SYNDROME

1 reference

12 December 2020

CHROMOSOME STUDIES IN SPONTANEOUS ABORTIONS

1 reference

12 December 2020

TRISOMY 17-18--AN EVALUATION OF PRECONCEPTIONAL PARENTAL IRRADIATION AS A POSSIBLE ETIOLOGIC FACTOR

1 reference

12 December 2020

Trisomy of chromosomes 13-15 and 17-18: its association with infantile arteriosclerosis

1 reference

12 December 2020

The 18-trisomy syndrome-two new clinical variants. One with associated tracheoesophageal fistula and the other with probable familial occurrence

1 reference

12 December 2020

[On a case of 17 trisomy.]

1 reference

12 December 2020

The No. 18 trisomy syndrome

1 reference

12 December 2020

1 reference

12 December 2020

Multiple congenital anomaly associated with an extra autosome

1 reference

12 December 2020

[Human chromosomes in tissue cultures]

1 reference

12 December 2020

AUTOSOMAL ABNORMALITIES

1 reference

12 December 2020

AUTOSOMAL TRISOMY SYNDROMES, EXCLUDING DOWN'S

1 reference

12 December 2020

THE NONRANDOMNESS OF CHROMOSOMAL ABNORMALITIES. ASSOCIATION OF TRISOMY 18 AND DOWN'S SYNDROME

1 reference

12 December 2020

TRISOMY 17-18(E): STUDIES IN LONG-TERM SURVIVAL WITH REPORT OF TWO AUTOPSIED CASES

1 reference

12 December 2020

THE PATHOLOGY OF 18 TRISOMY

1 reference

12 December 2020

TRISOMY 18 SYNDROME WITH ABSENT RADIUS, VARUS DEFORMITY OF HAND, AND RUDIMENTARY THUMB: REPORT OF A CASE

1 reference

12 December 2020

DEOXYRIBOSE-NUCLEIC-ACID REPLICATION PATTERN OF TRISOMY 18

1 reference

12 December 2020

THE 17-18 TRISOMY AND 21 TRISOMY SYNDROMES IN SIBLINGS

1 reference

12 December 2020

CONGENITAL ANOMALIES IN THE NEWBORN INFANT, INCLUDING MINOR VARIATIONS. A STUDY OF 4,412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES AND BUCCAL SMEAR FOR SEX CHROMATIN

1 reference

12 December 2020

TRISOMY 18. REPORT OF A CASE AND DISCUSSION OF THE SYNDROME

1 reference

12 December 2020

THE NO. 17-18 (E) TRISOMY SYNDROME. STUDIES ON CYTOGENETICS, DERMATOGLYPHICS, PATERNAL AGE, AND LINKAGE

1 reference

12 December 2020

Trisomy 18 (16-18) associated with congenital glaucoma and optic atrophy

1 reference

12 December 2020

Observations on the pathology of the trisomy 17-18 syndrome

1 reference

12 December 2020

The 16-18 trisomy syndrome

1 reference

12 December 2020

[The clinical aspects of common chromosomal abnormalities]

1 reference

12 December 2020

Identifiers

PMCID

1706095

1 reference

7 August 2017

1 reference

PubMed ID

17948514