Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 1 (of 1 Records) |
Query Trace: Brachyolmia[original query] |
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Bi-allelic loss-of-function novel variants in LTBP3-related skeletal dysplasia: Report of first patient from India. American journal of medical genetics. Part A 2020 5 182 (8): 1944-1946. Kaur Ravneet, Siddiqui Ishrat, Mathur Vijay, Jana Manisha, Kabra Madhulika, Gupta Neer |
- Page last reviewed:Feb 1, 2024
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