Results 191 to 200 of about 62,351 (250)

Supplementary Material for: Fast Approach for Clarification of Chromosomal Aberrations by Using LM-PCR and FT-CGH in Leukaemic Sample

open access: gold, 2011
Kathleen Dittmann   +6 more
openalex   +1 more source

Severe Neurodevelopmental Disorder due to Klinefelter Syndrome and <i>CACNA1C</i> Variant: A Case Report. [PDF]

open access: yesCase Rep Pediatr
El Kamel El Lebbi I   +5 more
europepmc   +1 more source

22q13.3 deletion syndrome: Clinical and molecular analysis using array CGH

open access: green, 2010
Shweta U. Dhar   +20 more
openalex   +2 more sources

PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion. [PDF]

open access: yesSci Rep
Vimercati A   +11 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy