(Q34814256)

4 August 2017

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title

Congenital chromosomal syndromes. A model for pathogenesis (English)

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4 August 2017

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Rohde RA

1

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4 August 2017

publication date

1 October 1965

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4 August 2017

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4 August 2017

volume

103

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4 August 2017

issue

4

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4 August 2017

page(s)

249-253

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DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME

4 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1515918

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1515918

The relationship between congenital anomalies and autosomal chromosome abnormalities

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1515918

Genetic regulatory mechanisms in the synthesis of proteins

8 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1515918

8 July 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1515918

FAMILIAL CHROMOSOME-2, 3 TRANSLOCATION ASCERTAINED THROUGH AN INFANT WITH MULTIPLE MALFORMATIONS.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1515918

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1515918

Production of congenital anomalies in mammals by maternal dietary deficiencies

26 October 2018

1 reference

12 December 2020

FOETAL HAEMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROME

1 reference

12 December 2020

THE LYON HYPOTHESIS AND FURTHER MALFORMATION POSTULATES IN THE CHROMOSOMAL SYNDROMES

1 reference

12 December 2020

Down's syndrome (mongolism) with normal chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

POTTER'S SYNDROME: CHROMOSOME ANALYSIS OF THREE CASES WITH POTTER'S SYNDROME OR RELATED SYNDROMES

1 reference

12 December 2020

MATERNAL TRANSMISSION OF A NEW GROUP-C(6/9) CHROMOSOMAL SYNDROME

1 reference

12 December 2020

DERMATOGLYPHIC ANOMALIES IN TURNER'S SYNDROME

1 reference

12 December 2020

THE EXCRETION OF TRYPTOPHAN METABOLITES FOLLOWING DEOXYPYRIDOXINE ADMINISTRATION IN MONGOLOID AND NONMONGOLOID PATIENTS

1 reference

12 December 2020

Identifiers

PMC publication ID

1515918

1 reference

4 August 2017

1 reference