(Q28249917)

English

Yunis Varon syndrome

scientific article

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

0 references

Yunis Varon syndrome (English)

0 references

author name string

M L Kulkarni

1

0 references

H N Vani

2

0 references

K Nagendra

3

0 references

T K Mahesh

4

0 references

Anand Kumar

5

0 references

Suja Haneef

6

0 references

Zaheeruddin Mohammed

7

0 references

Preethi M Kulkarni

8

0 references

language of work or name

0 references

publication date

April 2006

0 references

Indian Journal of Pediatrics

1 reference

73

0 references

4

0 references

353-5

0 references

Cleidocranial Dysostosis, Severe Micrognathism, Bilateral Absence of Thumbs and First Metatarsal Bone, and Distal Aphalangia

1 reference

https://api.crossref.org/works/10.1007%2FBF02825832

21 January 2018

Congenital heart malformation in Yunis-Varón syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypodontia, impacted permanent teeth, spinal defects, and cardiomegaly in a previously diagnosed case of the Yunis-Varon syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief clinical report: the syndrome of Yunis and Varón--report of a further case

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Yunis-Varon syndrome: evidence for a lysosomal storage disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generalized lysosomal storage in Yunis Varón syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atrophy of the left lobe of the liver and anomalous hepatic vessel in a patient with Yunis-Varon syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Yunis-Varon syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cleidocranial dysostosis, severe micrognathism, bilateral absence of thumbs and first metatarsal bone, and distal aphalangia: a new genetic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Yunis-Varon syndrome: the first case of German origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cleidocranial dysplasia with neonatal death due to central nervous system injury in utero: case report and literature review

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Yunis-Varon syndrome with severe osteodysplasty

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aplasia of the thumbs and great toes as the outstanding feature of Yunis and Varon syndrome. A new entity. A new observation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further delineation of the Yunis-Varon syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02825832

0 references

PubMed publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28249917&oldid=2175155019"