(Q50894375)

English

[Karyotype-phenotype correlation in a 46,Xdel(X) (p22) diagnosis (author's transl)].

scientific article published in March 1976

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scholarly article

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

[Karyotype-phenotype correlation in a 46,Xdel(X) (p22) diagnosis (author's transl)]. (English)

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

0 references

1 reference

based on heuristic

inferred from title

author name string

M Bartsch-Sandhoff

1

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

R Terinde

2

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

W Weigelmann

3

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

W Scholz

4

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

publication date

1 March 1976

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

31

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

263-270

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

3

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

https://scigraph.springernature.com/pub.10.1007/bf00270856

0 references

Abnormalities of human sex chromosomes. II. Turner's syndrome associated with the mosaicism 45,X-46, XX-p

1 reference

https://pubmed.ncbi.nlm.nih.gov/955625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Partial deletion of the short arm of an X chromosome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/955625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On a case of XXdc ovarian dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/955625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS

1 reference

https://pubmed.ncbi.nlm.nih.gov/955625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital anomalies associated with gonadal aplasia; review of 55 cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/955625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An inhertited X‐autosome translocation in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/955625

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/955625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00270856

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/955625

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