Chondrodysplasia punctata with X;Y translocation-Reference-Cited by-同舟云学术

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Chondrodysplasia punctata with X;Y translocation

Published:1988-09 Issue:1 Volume:80 Page:105-107
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Agematsu Kazunaga,Koike Kenichi,Morosawa Hironori,Nakahori Yutaka,Nakagome Yasuo,Akabane Taro

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00451470.pdf

Reference19 articles.

1. Akatsuka A, Nishiva O, Kitagawa T, Kageyama A, Inana I, Nakagome Y (1979) Trisomy 9 mosaicism with punctate mineralization in developing cartilages. Eur J Pediatr 131:271?275

2. Åkesson HO, Hagberg B, Wahlstrom J (1980) Y-to-X chromosome translocation observed in two generations. Hum Genet 55:39?42

3. Curry CJR, Magenis RE, Brown M, Lanmn JT, Tsai J, O'Lague P, Goodfellow P, Mohandas T, Bergner E, Shapiro LJ (1984) Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome. N Engl J Med 311:1010?1015

4. Gilbert EF, Opitz JM, Spranger JW, Langer LO, Wolfson JJ, Viseskul C (1976) Chondrodysplasia punctata-rhizomeric form. Eur J Pediatr 123:89?109

5. Happle R, Phillips RJS, Roessner A, Junemann G (1983) Homologous genes for X-linked chondrodysplasia punctata in man and mouse. Hum Genet 63:24?27

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1. Long-term follow-up of females with unbalanced X;Y translocations—reproductive and nonreproductive consequences;Molecular Cytogenetics;2015-02-22

2. Disorders of Keratinization;Rook's Textbook of Dermatology;2010-05-06

3. Chondrodysplasia punctata: a clinical diagnostic and radiological review;Clinical Dysmorphology;2008-10

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5. Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardation;Clinical Genetics;2005-02-22

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