(Q33676414)

28 July 2017

Severe intrauterine growth retardation with increased mitomycin C sensitivity: a further chromosome breakage syndrome (English)

1 reference

intrauterine growth restriction

28 July 2017

1 reference

Woods CG

1

1 reference

28 July 2017

Leversha M

series ordinal

2

1 reference

28 July 2017

Rogers JG

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 April 1995

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

32

1 reference

28 July 2017

301-305

1 reference

28 July 2017

4

1 reference

Familial dwarfism associated with microcephaly, mental retardation and anaemia

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Mammalian DNA-repair genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Acute myeloid leukaemia in a patient with Seckel syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

DNA repair genes and proteins of Saccharomyces cerevisiae

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Bird-beaded dwarfs (Seckel's syndrome). A familial pattern of developmental, dental, skeletal, genital, and central nervous system anomalies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Seckel syndrome: an overdiagnosed syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Fatal aplastic anaemia in a child with features of Dubowitz syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Cloning of cDNAs for Fanconi's anaemia by functional complementation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Seckel's Dwarfism: Analysis of Chromosome Breakage and Sister Chromatid Exchanges

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050381

Constitutional hypoplastic anemia associated with familial "bird-headed" dwarfism (Seckel syndrome)

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7643362

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Aplastic anemia associated with "bird-headed" dwarfism (Seckel syndrome)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7643362

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.32.4.301

1 reference

28 July 2017

1 reference

28 July 2017

1 reference