Results 181 to 190 of about 73,884 (236)

Characterisation of the MID1/α4 multiprotein complex

open access: yes, 2006
Opitz BBB/G syndrome (OS) is a congenital disorder characterised by malformations of the ventral midline, with hypertelorism and hypospadias being the two cardinal phenotypic manifestations. OS is genetically heterogeneous, with an autosomal and an X-linked locus.
openaire   +1 more source

Very Stable High-Molecular-Mass Multiprotein Complexes in Different Organs of the Sea Cucumber <i>Paracaudina chilensis</i>. [PDF]

open access: yesMolecules
Soboleva SE   +5 more
europepmc   +1 more source

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