Results 131 to 140 of about 19,510 (212)

Delineation of a complex karyotypic rearrangement by microdissection and CGH in a family affected with split foot. [PDF]

open access: yesJ Med Genet, 2000
Weimer J   +7 more
europepmc   +1 more source

Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum. [PDF]

open access: yesJ Med Genet, 1970
Fischer P   +5 more
europepmc   +1 more source

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