Results 41 to 50 of about 171 (84)

Intronic hexanucleotide repeat expansion in <i>TYMS</i> in monozygotic twins with congenital progressive universal melanosis. [PDF]

open access: yesBiomed Rep
Kanchanasutthiyakorn S   +10 more
europepmc   +1 more source

Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia

open access: yesOur Dermatology Online
Sheenu Goyal   +3 more
openaire   +1 more source

Dyskeratosis congenita: a rare case report. [PDF]

open access: yesOxf Med Case Reports
Khattab S   +3 more
europepmc   +1 more source

Salzmann Nodular Degeneration in Ocular and Systemic Diseases. [PDF]

open access: yesJ Clin Med
Roszkowska AM   +6 more
europepmc   +1 more source

Blistering and Mottled Pigmentation in a Young Male. [PDF]

open access: yesIndian Dermatol Online J, 2018
Bains A   +3 more
europepmc   +1 more source

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