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Haploinsufficiency of NKX2-1 is likely to contribute to developmental delay involving 14q13 microdeletions. [PDF]

open access: yesIntractable Rare Dis Res
Machida O   +10 more
europepmc   +1 more source

Gardner syndrome: When cervical-facial osteomas reveal the tip of the iceberg: A case report and literature review. [PDF]

open access: yesRadiol Case Rep
Andour H   +6 more
europepmc   +1 more source
Some of the next articles are maybe not open access.

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ECTODERMAL DYSPLASIA WITH TRUE ANODONTIA-A RARE CASE REPORT

International journal of scientific research, 2023
Ectodermal dysplasia is a genetic disorder caused by defects in the ectoderm that is developing in the embryo. The distinction between the hidrotic and hypo hidrotic kinds of ectodermal dysplasia is based on the presence or lack of sweat glands.
Sameeksha Bhardwaj   +5 more
semanticscholar   +1 more source

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