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Links from Nucleotide

Items: 4

1.
A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter–Thompson type
Asmat Ullah, Muhammad Umair, Dost Muhammad, Muhammad Bilal, Kwanghyuk Lee, Suzanne M Leal, Wasim Ahmad
Ann Hum Genet. Author manuscript; available in PMC 2018 Sep 17.
Published in final edited form as: Ann Hum Genet. 2018 May; 82(3): 129–134. Published online 2018 Jan 10. doi: 10.1111/ahg.12233
PMCID:
PMC6141004
ArticlePDF–983K
2.
Linked homozygous BMPR1B and PDHA2 variants in a consanguineous family with complex digit malformation and male infertility
Yeşerin Yıldırım, Toufik Ouriachi, Ute Woehlbier, Wahiba Ouahioune, Mahmut Balkan, Sajid Malik, Aslıhan Tolun
Eur J Hum Genet. 2018 Jun; 26(6): 876–885. Published online 2018 Mar 26. doi: 10.1038/s41431-018-0121-7
PMCID:
PMC5973948
ArticlePDF–1.4M
3.
BMPR1B mutation causes Pierre Robin sequence
Yongjia Yang, Jianying Yuan, Xu Yao, Rong Zhang, Hui Yang, Rui Zhao, Jihong Guo, Ke Jin, Haibo Mei, Yongqi Luo, Liu Zhao, Ming Tu, Yimin Zhu
Oncotarget. 2017 Apr 18; 8(16): 25864–25871. Published online 2017 Mar 23. doi: 10.18632/oncotarget.16531
PMCID:
PMC5432222
ArticlePDF–1.8M
4.
Bone morphogenetic protein type IB receptor is progressively expressed in malignant glioma tumours.
N. Yamada, M. Kato, P. ten Dijke, H. Yamashita, T. K. Sampath, C. H. Heldin, K. Miyazono, K. Funa
Br J Cancer. 1996 Mar; 73(5): 624–629. doi: 10.1038/bjc.1996.108
PMCID:
PMC2074358
ArticlePDF–1.6M

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