(Q51948729)

18 April 2018

reason for preferred rank

title

Malignant hematological disorders in children with Wolf–Hirschhorn syndrome (English)

1 reference

https://api.crossref.org/works/10.1002/AJMG.A.20080

2 January 2024

Malignant hematological disorders in children with Wolf-Hirschhorn syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12749063

2 January 2024

1 reference

https://api.crossref.org/works/10.1002/AJMG.A.20080

2 January 2024

7

Yigal Dror

1 reference

18 April 2018

Melvin H Freedman

3

object named as

Melvin Freedman

1 reference

18 April 2018

author name string

Anjali Sharathkumar

1

1 reference

18 April 2018

Melanie Kirby

2

1 reference

18 April 2018

Mohamed Abdelhaleem

4

1 reference

18 April 2018

David Chitayat

5

1 reference

18 April 2018

Melvin Freedman

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12749063

2 January 2024

Ikuko E. Teshima

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12749063

2 January 2024

language of work or name

English

0 references

publication date

1 June 2003

1 reference

18 April 2018

full work available at URL

https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajmg.a.20080

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12749063

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.a.20080

2 January 2024

1 reference

https://api.crossref.org/works/10.1002/AJMG.A.20080

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.20080

2 January 2024

1 reference

https://api.crossref.org/works/10.1002/AJMG.A.20080

American Journal of Medical Genetics

2 January 2024

published in

1 reference

18 April 2018

volume

119A

1 reference

18 April 2018

issue

2

1 reference

18 April 2018

page(s)

194-199

1 reference

18 April 2018

Clinical significance of the del(20q) chromosome in hematologic disorders

cites work

https://api.crossref.org/works/10.1002/AJMG.A.20080

1

1 reference

Deletions of chromosome 20q and the pathogenesis of myeloproliferative disorders

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

2

1 reference

Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

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1 reference

Myelodysplastic syndromes in childhood: report of 49 patients from a French multicentre study. French Society of Paediatric Haematology and Immunology

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

4

1 reference

The FGF family of growth factors and oncogenes

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

5

1 reference

Natural history of Wolf-Hirschhorn syndrome: experience with 15 cases

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

6

1 reference

Malignant myeloid transformation with isochromosome 7q in Shwachman-Diamond syndrome

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

7

1 reference

Clonal evolution in marrows of patients with Shwachman-Diamond syndrome: a prospective 5-year follow-up study.

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

8

1 reference

Myelodysplasia and myeloproliferative disorders in childhood: an update

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

9

1 reference

Preliminary phenotypic map of chromosome 4p16 based on 4p deletions.

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

10

1 reference

Digitized and differentially shaded human chromosome ideograms for genomic applications.

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

12

1 reference

Forty-four cases of childhood myelodysplasia with cytogenetics, documented by the Groupe Français de Cytogénétique Hématologique

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

13

1 reference

Thrombocytosis with sideroblastic erythropoiesis: a mixed myeloproliferative myelodysplastic syndrome

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

14

1 reference

Acute lymphoid leukemias following either a previous chronic myelogenous leukemia or myelodysplastic syndrome: phenotypic and genomic differences.

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

15

1 reference

Assignment of the human GATA4 gene to 8p23.1-->p22 using fluorescence in situ hybridization analysis

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

17

1 reference

Structural and Functional Diversity in the FGf Receptor Multigene Family

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

18

1 reference

The Wolf-Hirschhorn (4p-) syndrome.

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

19

1 reference

Transformation of chronic myelomonocytic leukemia to acute lymphoblastic leukemia: case report and review of the literature of lymphoblastic transformation of myelodysplastic syndrome

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

20

1 reference

A practical, comprehensive classification for pediatric myelodysplastic syndromes: the CCC system.

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

22

1 reference

Modulation of WHSC2 expression in human endothelial cells

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

23

1 reference

Fibroblast-growth-factor receptor mutations in human skeletal disorders

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

24

1 reference

Interphase detection of t(4;14)(p16.3;q32.3) by in situ hybridization and FGFR3 overexpression in plasma cell malignancies

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

25

1 reference

GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

26

1 reference

Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

27

1 reference

An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

29

1 reference

Deletions of chromosome 4 occur early during the pathogenesis of colorectal carcinoma

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

31

1 reference

Loss of heterozygosity at 4p16.3 and mutation of FGFR3 in transitional cell carcinoma.

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

32

1 reference

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

33

1 reference

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

34

1 reference

Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

35

1 reference

A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4.

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

36

1 reference

A zinc-finger gene ZNF141 mapping at 4p16.3/D4S90 is a candidate gene for the Wolf-Hirschhorn (4p-) syndrome

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

37

1 reference

Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

38

1 reference

Assignment of the transcription factor GATA4 gene to human chromosome 8 and mouse chromosome 14: Gata4 is a candidate gene for Ds (disorganization).

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

39

1 reference

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

40

1 reference

Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)]

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

41

1 reference

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

43

1 reference

Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling, fluorescence in situ hybridization, and conventional cytogenetic analyses. A study of 54 cases with hematological disorders

2 January 2024

https://api.crossref.org/works/10.1002/AJMG.A.20080

44

1 reference

2 January 2024

Identifiers

DOI

10.1002/AJMG.A.20080

1 reference

18 April 2018

1 reference

18 April 2018