(Q34448661)

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Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter?

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Europe PubMed Central

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2 August 2017

Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter? (English)

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Europe PubMed Central

PubMed publication ID

2 August 2017

focal dermal hypoplasia

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inferred from title

author name string

Zuffardi O

1

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Europe PubMed Central

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2 August 2017

Caiulo A

2

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Europe PubMed Central

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2 August 2017

Maraschio P

3

1 reference

Europe PubMed Central

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2 August 2017

Tupler R

4

1 reference

Europe PubMed Central

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2 August 2017

Bianchi E

5

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Europe PubMed Central

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2 August 2017

Amisano P

6

1 reference

Europe PubMed Central

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2 August 2017

Beluffi G

7

1 reference

Europe PubMed Central

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2 August 2017

Moratti R

8

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2 August 2017

Liguri G

9

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2 August 2017

publication date

1 April 1989

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2 August 2017

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2 August 2017

82

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2 August 2017

1

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2 August 2017

17-19

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2 August 2017

Data on the incidence, segregation and linkage relations of the adenylate kinase (AK) polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked dominant inherited diseases with lethality in hemizygous males

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Focal dermal hypoplasia syndrome. Case report and literature review

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inverted tandem (“mirror”) duplications in human chromosomes: Inv dup 8p, 4q, 22q

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An interstitial deletion of chromosome 9 in a girl with multiple congenital anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 4q in two unrelated cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of ABO locus to 9q31.3----qter by study of a family in which an intrachromosomal shift involving chromosome 9 is segregating

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of the loci for the nail-patella syndrome and adenylate kinase

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of human alpha 1 acid glycoprotein genes to 9q31----34.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intercalary deletions of 9q

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A chromosomal break and partial deletion of a number 9 chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2541064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00288264

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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