(Q54237720)

English

A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21.

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scholarly article

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21. (English)

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

craniosynostosis

0 references

author name string

T Motegi

1

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

M Ohuchi

2

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

C Ohtaki

3

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

K Fujiwara

4

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

S Enomoto

5

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

T Hasegawa

6

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

K Kishi

7

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

H Hayakawa

8

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

publication date

1 January 1985

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

71

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

160-162

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

2

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

https://scigraph.springernature.com/pub.10.1007/bf00283374

0 references

Terminal 7p deletion and 1;7 translocation associated with craniosynostosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial, balanced insertional translocation of chromosome 7 leading to offspring with deletion and duplication of the inserted segment, 7p15 → 7p21

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A girl with karyotype 46,XX,del(7) (qter?p15:)

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A patient with interstitial deletion 7 (p13 leads to p21)

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 7 short-arm interstitial deletion (p14)

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring chromosome 7 with variable phenotypic expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome banding

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation, malformation syndrome andpartial 7p monosomy [45, XX, tdic (7;15) (p21;p11)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial deletion of the short arm of chromosome 7 without craniosynostosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Giant satellites or translocation?

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of the short arm of chromosome 7 without craniosynostosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/4043965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00283374

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/4043965

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