X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter (Q71083985)

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scientific article published on 01 January 1981

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English	X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter	scientific article published on 01 January 1981

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scholarly article

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16 October 2019

X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter (English)

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16 October 2019

human chromosomes 6-12 and X

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10 May 2024

chromosomal translocation

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10 May 2024

Charles Edmund Ford

4

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C. E. Ford

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10 May 2024

author name string

K. Madan

1

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10 May 2024

P. G. Hompes

2

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10 May 2024

J. Schoemaker

3

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10 May 2024

language of work or name

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National Center for Biotechnology Information

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10 May 2024

publication date

1 January 1981

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16 October 2019

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00295460.pdf

Portable Document Format

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10.1007/BF00295460

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10 May 2024

http://link.springer.com/article/10.1007/BF00295460/fulltext.html

1 reference

10.1007/BF00295460

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http://link.springer.com/content/pdf/10.1007/BF00295460

1 reference

10.1007/BF00295460

https://api.crossref.org/works/10.1007/BF00295460

10 May 2024

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16 October 2019

59

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16 October 2019

4

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16 October 2019

290-296

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Europe PubMed Central

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16 October 2019

X-autosome translocations: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Typical Turner's syndrome with 45 XO karyotype and normal menstruation. Cytogenetic and histological findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-autosome translocations in the mouse: total inactivation versus partial inactivation of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gonadal dysgenesis in a patient with an X;3 translocation: case report and review

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two human X-autosome translocations identified by autoradiography and fluorescence

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombinant chromosome as a result of pericentric inversion of X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible X-autosomal translocation in a girl with gonadal dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation in association with a balanced X-autosome translocation and random inactivation of the X chromosomes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A FAMILY APPARENTLY SHOWING TRANSMISSION OF A TRANSLOCATION BETWEEN CHROMOSOME 3 AND ONE OF THE 'X-6-12' OR 'C' GROUP

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An (X;1) translocation, balanced, 46 chromosomes. Repository identification no. GM-97.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication pattern of the X chromosomes in three X/autosomal translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic and clinical study on 100 cases of primary amenorrhoea

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-autosome translocation in normal mother and effectively 21-monosomic daughter.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X inactivation pattern in an unbalanced X-autosome translocation with gonadal dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Follow-up on a human X-autosome translocation first studied in 1963 and 1964

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for the existence of the human "super female".

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A CASE OF PRIMARY AMENORRHEA WITH A TRANSLOCATION INVOLVING CHROMOSOMES OF GROUPS B AND C

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[X-chromosome translocations. Examination based on treatment with BUDR and staining with acridine orange]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late replication and X-autosome traslocation a case with banding patterns autoradiographic and B.U.D.R. studies (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-inactivation pattern in three cases of X/autosome translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secondary amenorrhea associated with balanced X-autosome translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Banding patterns and autoradiographic studies of cells with an X-autosome translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial X-22 translocation with an extra X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

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/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

45,X lymphocyte karyotype in a fertile woman

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spreading of inactivation in an (X;14) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further observations on a 13qXp translocation associated with retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Semen analysis in subfertile balanced-translocation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An analysis of the break points of structural rearrangements in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

45,XO Turner's syndrome without evidence of mosaicism in a patient with two pregnancies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-short arm deletion gonadal dysgenesis in two siblings due to unique translocation (Xp-;16p+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four new cases of X-autosome translocation in man (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Numerical abnormalities of the X chromosome. Frequency among inpatients of a general hospital and in a general population

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytogenetic survey of men being investigated for subfertility

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Letter: A case of primary amenorrhea associated with X-autosomal translocation (46,X,t(Xq minus;5q plus))

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presumptive evidence of two active X chromosomes in somatic cells of a human female

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex-Linked Recessive Lethals in Drosophila Whose Expression Is Suppressed by the Y Chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure of X inactivation in the autosomal segment of an X/A translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 4q syndrome: case report and review

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reinvestigation of two X/autosome translocations:segregation in cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intrachromosomal gene mapping in man: assignment of nucleoside phosphorylase to region 14cen leads to 14q21 by interspecific hybridization of cells with a t(X;14) (p22;q21) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of partial trisomy 17 resulting from X-autosomal translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Balanced reciprocal X-4 translocation in a female patient with early secondary amenorrhea

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A reciprocal translocation (X;11) in a female with gonadal dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aspermia, associated with a presumably balanced X/autosomal translocation karyotype 46, Y, t (X;5) (q28;q11)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural X-chromosome abnormality in a female with gonadal dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A dynamic study in two new cases of X chromosome translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/7333583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical Genetics

13

17

61

author name string

C Cuoco

publication date

1980

1 reference

10.1007/BF00295460

https://api.crossref.org/works/10.1007/BF00295460

10 May 2024

Helvetica paediatrica acta

16

34

19

author name string

B Dutrillaux

publication date

1974

1 reference

10.1007/BF00295460

https://api.crossref.org/works/10.1007/BF00295460

10 May 2024

Helvetica paediatrica acta

25

30

281

author name string

Y Gilboa

publication date

1975

1 reference

10.1007/BF00295460

https://api.crossref.org/works/10.1007/BF00295460

10 May 2024

Clinical Genetics

30

13

118

author name string

CB Hagen van der

publication date

1978

1 reference

10.1007/BF00295460

https://api.crossref.org/works/10.1007/BF00295460

10 May 2024

Identifiers

10.1007/BF00295460

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7333583%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7333583%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

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