X long-arm deletions. A review of non-mosaic cases studied with banding techniques (Q40242358)

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scientific article published on January 1984

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English	X long-arm deletions. A review of non-mosaic cases studied with banding techniques	scientific article published on January 1984

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

title

X long-arm deletions. A review of non-mosaic cases studied with banding techniques (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

author

Henrik Westh

object named as

H Westh

series ordinal

2

0 references

author name string

L Skibsted

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

E Niebuhr

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

publication date

1 January 1984

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

volume

67

1 reference

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Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

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18 September 2017

page(s)

1-5

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Europe PubMed Central

PubMed publication ID

6745919

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18 September 2017

cites work

Metacarpophalangeal pattern profiles in the evaluation of skeletal malformations.

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FBF00270550

retrieved

21 January 2018

X inactivation in man: a woman with t(Xq--;12q+)

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-autosome translocations: cytogenetic characteristics and their consequences

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

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inferred from PubMed ID database lookup

Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X chromosome constitution and the human female phenotype

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete deletion of long arm of X chromosome in woman without Turner syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Women heterozygous for deficiency of the (p21 ? pter) region of the X chromosome are fertile

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

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[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)]

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A teen-ager with 46,X,del(X)(q21)

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial long arm deletion of one X chromosome in a patient with secondary amenorrhea

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

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Topological classification of palmar dermatoglyphics

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X deletion and primary amenorrhoea

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence and autoradiographic studies in patients with Turner's syndrome and 46,XXp- and 46,XXq- karyotypes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased Q fluorescence of an inactive Xq-chromosome in man

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Premature menopause due to a small deletion in the long arm of the X chromosome: a report of three cases and a review

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural anomalies of the X chromosome: personal observation and review of non-mosaic cases.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gonadal dysgenesis and X chromosome deletion. Case reports

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Position of the human X inactivation center on Xq

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter)

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fertility in patients with X chromosome deletions

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features of a patient with 46, XXq- and genetic inactivaiton of the X chromosome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief clinical report: del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gonadal dysgenesis and abnormalities of the human sex chromosomes: current status of phenotypic-karyotypic correlations

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and cytogenetic aspects of X-chromosome deletions

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytologic and molecular analysis of 46,XXq- cells to identify a DNA segment that might serve as a probe for a putative human X chromosome inactivation center.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X LONG-ARM DELETION WITH FEATURES OF TURNER'S SYNDROME

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion mapping of the human X chromosome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X long arm deletion with oligomenorrhoea.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Turner syndrome with partial deletion of the X chromosome long arm

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation of an X ring chromosome in two generations.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 5/X chromosomal translocation in a patient with premature menopause

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6745919

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00270550

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

Dimensions Publication ID

1003479057

0 references

PubMed publication ID

6745919

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745919

retrieved

18 September 2017

 

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