(Q33669958)

28 July 2017

Spectrum of anomalies in Fanconi anaemia (English)

1 reference

28 July 2017

Glanz A

1

1 reference

PubMed ID

7154038

28 July 2017

Fraser FC

series ordinal

2

1 reference

PubMed ID

7154038

28 July 2017

language of work or name

English

0 references

publication date

1 December 1982

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

19

1 reference

28 July 2017

412-416

1 reference

28 July 2017

6

1 reference

Congenital pancytopenia associated with multiple congenital anomalies (Fanconi type); review of the literature and report of a twenty-year-old female with a ten-year follow-up and apparently good response to splenectomy

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

The value of splenectomy in Fanconi's anaemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

A case of Fanconi's syndrome with a study of peroxidase activity of the erythron

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

The numerical versus intuitive approach to syndrome nosology.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Clinical and chromosome studies in Fanconi's aplastic anaemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Constitutional aplastic anaemia (Fanconi type): case presentation and review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Squamous Cell Carcinomas in Fanconi's Anemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Fanconi's anemia with growth hormone deficiency.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Disorders of Bone Marrow Production

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

21 June 2018

Fanconi anemia syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Chromosomal aberrations in two cases of inherited aplastic anemia with unusual clinical features.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Nonrandom distribution of chromosome breaks in Fanconi's anemia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Fanconi's anemia. I. Case histories, clinical and laboratory findings in six affected siblings

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Fanconi's aplastic anaemia: a case report of an affected African child and a review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Formal genetics of Fanconi's anemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Fanconi's anaemia, with special reference to erythrokinetic features

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Indication of primary immune deficiency in Fanconi's anemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Studies of malformation syndromes of man XL VII: Disappearance of spermatogonia in the fanconi anemia 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=1048952

Terminological, Diagnostic, Nosological, and Anatomical-Developmental Aspects of Developmental Defects in Man

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Cytogenetic studies in four cases of Fanconi's anemia (author's transl)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Localization of chromatid breaks in Fanconi's anemia, using three consecutive stains

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Fanconi's anaemia (aplastic anaemia with congenital abnormalities).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

Hypoplastic anemia with multiple congenital defects (Fanconi syndrome).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048952

[Familial hypoplastic anaemia with congenital abnormalities (Fanconi's syndrome): report of a case]

30 October 2018

1 reference

12 December 2020

Fanconi anemia: Simultaneous onset of symptoms in two siblings

1 reference

12 December 2020

Congenital hypoplastic anemia associated with multiple developmental defects (Fanconi's syndrome)

1 reference

12 December 2020

Familial hypoplastic anemia with multiple congenital anomalies (Fanconi's syndrome)--report of three cases. Cases presented are of two sisters and a female cousin with complete clinical and post mortem findings

1 reference

12 December 2020

Fanconi's anemia. Report of 3 cases

1 reference

12 December 2020

Familial cancer on a Scottish island

1 reference

12 December 2020

Transposition of external genitalia in a case with Fanconi type deformity

1 reference

12 December 2020

[Fanconi type dwarfism with terminal aplastic myelosis]

1 reference

12 December 2020

Chronic Pancytopenia with Multiple Congenital Abnormalities (Fanconi's Anaemia)

1 reference

12 December 2020

Letter: Fanconi's anemia in offspring of patient with congenital radial and carpal hypoplasia

1 reference

12 December 2020

Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects

1 reference

12 December 2020

Constitutional infantile panmyelopathy with multiple malformations Fanconi anemia

1 reference

12 December 2020

Familial pancytopenia with congenital abnormalities (Fanconi syndrome)

1 reference

12 December 2020

Chromosomal breaks in T and B lymphocytes in Fanconi's anemia

1 reference

12 December 2020

The coincidence of hemoglobin J and Fanconi's syndrome of hypoplastic anemia with hypoplasia of the spleen in a young man

1 reference

12 December 2020

Constitutional anemia (Fanconi's syndrome) and leukemia in two brothers

1 reference

12 December 2020

Fanconi syndrome; multiple congenital anomalies with hypoplastic anemia

1 reference

12 December 2020

Aplastic anemia in siblings with multiple congenital anomalies (the Fanconi type)

1 reference

12 December 2020

Somatic segregation and Fanconi anemia

1 reference

12 December 2020

[Family Pancytopenia]

1 reference

12 December 2020

Roentgen appearance of anomalies associated with hypoplastic anemias of childhood: Fanconi's anemia and congenital hypoplastic anemia (erythrogenesis imperfecta)

1 reference

12 December 2020

Distribution of chromosome breaks in measles, Fanconi's anemia and controls

1 reference

12 December 2020

Roentgenographic Findings in Fanconi's Anemia

1 reference

12 December 2020

Identifiers

PMCID

1048952

1 reference

28 July 2017

1 reference

PubMed ID

7154038