Chromosome 7 short arm deletion, 7p21----pter (Q56408412)

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Language	Label	Description	Also known as
English	Chromosome 7 short arm deletion, 7p21----pter	No description defined

Statements

scholarly article

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Chromosome 7 short arm deletion, 7p21----pter (English)

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author name string

M Schömig-Spingler

1

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M Schmid

2

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W Brosi

3

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T Grimm

4

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language of work or name

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publication date

November 1986

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74

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3

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323-5

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Hemihypotrophy in a girl with a translocation t(13q;7p)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3781561

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3781561

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple method for R banding of human chromosomes, showing a pH-dependent connection between R and G bands.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3781561

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/3781561

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/3781561

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/3781561

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/3781561

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/3781561

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3781561

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/3781561

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/3781561

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/3781561

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/3781561

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3781561

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Giant satellites or translocation?

1 reference

https://pubmed.ncbi.nlm.nih.gov/3781561

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/3781561

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/3781561

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00282559

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PubMed publication ID

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