A comparison of constitutive heterochromatin staining methods in two cases of familial heterochromatin deficiencies-Reference-Cited by-同舟云学术

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A comparison of constitutive heterochromatin staining methods in two cases of familial heterochromatin deficiencies

Published:1979 Issue:1 Volume:52 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Buys C.H.C.M.,Anders G.J.P.A.,Gouw W.L.,Borkent-Ypma J.M.M.,Blenkers-Platter J.A.M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00284607.pdf

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. ATAC-see reveals the accessible genome by transposase-mediated imaging and sequencing;Nature Methods;2016-10-17

2. Prader-Willi syndrome and a bisatellited derivative of chromosome 15;Clinical Genetics;2008-04-23

3. Absence of Pericentromeric Heterochromatin (9qh-) in a Patient with Bilateral Retinoblastoma;Acta geneticae medicae et gemellologiae: twin research;1997-10

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