(Q41644474)

6 October 2017

X chromosome constitution and the human female phenotype (English)

1 reference

6 October 2017

E Therman

1

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6 October 2017

C Denniston

series ordinal

2

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6 October 2017

G E Sarto

series ordinal

3

1 reference

6 October 2017

M Ulber

series ordinal

4

1 reference

6 October 2017

1 January 1980

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6 October 2017

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6 October 2017

54

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6 October 2017

133-143

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6 October 2017

2

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https://scigraph.springernature.com/pub.10.1007/bf00278961

6 October 2017

0 references

cites work

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Unreliability of the microcomplement fixation method for Xga typing of cultured fibroblasts

1 reference

12 December 2020

Reduced phenotypic effect on partial trisomy 1q in a X/1 translocation

1 reference

12 December 2020

The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.

1 reference

12 December 2020

Prognosis in newborn infants with X-chromosomal abnormalities

1 reference

12 December 2020

Position of the human X inactivation center on Xq

1 reference

12 December 2020

Abnormal X chromosomes in man: Origin, behavior and effects

1 reference

12 December 2020

THE LYON-BEUTLER HYPOTHESIS AND ISOCHROMOSOME X PATIENTS WITH TURNER SYNDROME

1 reference

12 December 2020

Spreading of inactivation in an (X;14) translocation

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical and cytological aspects of sex chromosome activity.

1 reference

12 December 2020

Two human X-autosome translocations identified by autoradiography and fluorescence

1 reference

12 December 2020

Trisomy 8: an international study of 70 patients

1 reference

12 December 2020

Structure and Barr body formation of an Xp + chromosome with two inactivation centers

1 reference

12 December 2020

Nonpairing of the X and Y chromosomes in the spermatocytes of BDF<sub>1</sub> mice

1 reference

12 December 2020

Familial gonadal dysgenesis

1 reference

12 December 2020

Unbalanced X-autosomal translocation with inactivation of the normal X chromosome

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytologic evidence for preferential inactivation of the paternally derived X chromosome in XX mouse blastocysts

1 reference

12 December 2020

Recombinant chromosome as a result of pericentric inversion of X chromosome

1 reference

12 December 2020

Trisomy 14 mosaicism: case report and review

1 reference

12 December 2020

Clustering of aberrations to specific chromosomes in human neoplasms. III. Incidence and geographic distribution of chromosome aberrations in 856 cases

1 reference

12 December 2020

Imbalance in X-chromosome expression: evidence for a human X-linked gene affecting growth of hemopoietic cells

1 reference

12 December 2020

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

1 reference

12 December 2020

Non-inactivation of an X-Chromosome Locus in Man

1 reference

12 December 2020

Replication and inactivation of a dicentric X formed by telomeric fusion

1 reference

12 December 2020

Familial incidence of pericentric inversion of X chromosome

1 reference

12 December 2020

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

1 reference

12 December 2020

A possible active segment on the inactive human X chromosome

1 reference

12 December 2020

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

1 reference

12 December 2020

X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies

1 reference

12 December 2020

Nullisomy for the distal portion of Xp in a male child with a X/Y translocation

1 reference

12 December 2020

Preferential X inactivation in human placenta membranes: is the paternal X inactive in early embryonic development of female mammals?

1 reference

12 December 2020

X-autosome translocations: a review

1 reference

12 December 2020

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

1 reference

12 December 2020

Both X chromosomes function before visible X-chromosome inactivation in female mouse embryos

1 reference

12 December 2020

Mechanisms and evolutionary origins of variable X-chromosome activity in mammals

1 reference

12 December 2020

Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy

1 reference

12 December 2020

An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.

1 reference

12 December 2020

BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes

1 reference

12 December 2020

Non-random inactivation of X chromosome in the rat yolk sac

1 reference

12 December 2020

Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

1 reference

12 December 2020

Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+

1 reference

12 December 2020

Penta X (49,XXXXX) chromosome constitution: a case report

1 reference

12 December 2020

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

1 reference

12 December 2020

In search of non-random X inactivation: studies of fetal membranes heterozygous for glucose-6-phosphate dehydrogenase

1 reference

12 December 2020

The Xga antigen on red cells and fibroblasts

1 reference

12 December 2020

Control of chromosome inactivation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00278961

1 reference

Dimensions Publication ID

6 October 2017

0 references

1 reference