Human Autosomal Recessive Osteopetrosis Maps to 11q13, a Position Predicted by Comparative Mapping of the Murine Osteosclerosis (oc) Mutation

C Heaney, H Shalev, K Elbedour… - Human molecular …, 1998 - academic.oup.com
Autosomal recessive osteopetrosis is a rare congenital disorder characterized by the
development of abnormally dense bones, acrocephaly, severe anemia …
被引用次数：110 相关文章
[PDF] psu.edu

[PDF][PDF] Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation

C Heaney, H Shalev, K Elbedour, R Carmi… - Human Molecular …, 1998 - Citeseer
Autosomal recessive osteopetrosis is a rare congenital disorder characterized by the
development of abnormally dense bones, acrocephaly, severe anemia …

Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation.

C Heaney, H Shalev, K Elbedour… - Human Molecular …, 1998 - search.ebscohost.com
Shows that human autosomal recessive osteopetrosis maps to 11q13, which is the region
that has conserved synteny with the position on chromosome 19 to which the mouse …

Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation

C Heaney, H Shalev, K Elbedour, R Carmi… - Human Molecular …, 1998 - cris.bgu.ac.il
Autosomal recessive osteopetrosis is a rare congenital disorder characterized by the
development of abnormally dense bones, acrocephaly, severe anemia …
[PDF] archive.org

[PDF][PDF] Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation

C Heaney, H Shalev, K Elbedour… - Human Molecular …, 1998 - scholar.archive.org
Autosomal recessive osteopetrosis is a rare congenital disorder characterized by the
development of abnormally dense bones, acrocephaly, severe anemia …

Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation.

C Heaney, H Shalev, K Elbedour, R Carmi… - Human Molecular …, 1998 - europepmc.org
Autosomal recessive osteopetrosis is a rare congenital disorder characterized by the
development of abnormally dense bones, acrocephaly, severe anemia …

[引用][C] Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation

C Heaney - Human Molecular Genetics, 1998 - cir.nii.ac.jp
Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative
mapping of the murine osteosclerosis (oc) mutation | CiNii Research CiNii 国立情報学研究所 …

Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation

C Heaney, H Shalev, K Elbedour, R Carmi… - Human molecular …, 1998 - iro.uiowa.edu
Autosomal recessive osteopetrosis is a rare congenital disorder characterized by the
development of abnormally dense bones, acrocephaly, severe anemia …

Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation

C Heaney, H Shalev, K Elbedour… - Human molecular …, 1998 - pubmed.ncbi.nlm.nih.gov
Autosomal recessive osteopetrosis is a rare congenital disorder characterized by the
development of abnormally dense bones, acrocephaly, severe anemia …
[PDF] researchgate.net

[PDF][PDF] Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation

C Heaney, H Shalev, K Elbedour, R Carmi… - Human Molecular …, 1998 - researchgate.net
Autosomal recessive osteopetrosis is a rare congenital disorder characterized by the
development of abnormally dense bones, acrocephaly, severe anemia …