Clinical Consequence of Xp-

Overview

Journal Hum Genet

Specialty Genetics

Date 1979 Feb 15

PMID 437780

Citations 6

Authors

J J Hoo

Affiliations

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Citing Articles

Partial short arm deletion of the X chromosome 46,X,del(X)(qter = to p21:).

Kaosaar M, Mikelsaar A Hum Genet. 1980; 53(2):275-7.

PMID: 7358395 DOI: 10.1007/BF00273511.

The various phenotypes in Xp deletion. observations in eleven patients.

Fryns J, Petit P, Van Den Berghe H Hum Genet. 1981; 57(4):385-7.

PMID: 7286978 DOI: 10.1007/BF00281690.

Segregation of an X ring chromosome in two generations.

Dallapiccola B, Bruni L, Boscherini B, Pasquino A, Chessa L, VIGNETTI P J Med Genet. 1980; 17(4):306-8.

PMID: 7205906 PMC: 1048575. DOI: 10.1136/jmg.17.4.306.

Clinical consequences of Xp-.

Egozcue J Hum Genet. 1980; 55(1):141-2.

PMID: 7192687 DOI: 10.1007/BF00329143.

Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2.

Allanson J, Richter S J Med Genet. 1991; 28(2):143-4.

PMID: 2002490 PMC: 1016789. DOI: 10.1136/jmg.28.2.143-a.

References

Terinde R, Weigelmann W, Scholz W . [Karyotype-phenotype correlation in a 46,Xdel(X) (p22) diagnosis (author's transl)]. Hum Genet. 1976; 31(3):263-70. DOI: 10.1007/BF00270856. View

Hoo J . Letter: Evolution of X-chromosome inactivation. Lancet. 1976; 1(7956):434. DOI: 10.1016/s0140-6736(76)90285-3. View

Hoo J . Letter: Cytogenetic evidence for evolution of X-chromosome inactivation. Lancet. 1975; 1(7919):1299-300. DOI: 10.1016/s0140-6736(75)92586-6. View

THERMAN E, Sarto G, Disteche C, Denniston C . A possible active segment on the inactive human X chromosome. Chromosoma. 1976; 59(2):137-45. DOI: 10.1007/BF00328482. View

Hecht F, Jones D, Delay M, Klevit H . Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome. J Med Genet. 1970; 7(1):1-4. PMC: 1468913. DOI: 10.1136/jmg.7.1.1. View