Matches in Nanopublications for { ?s ?p "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523009.RA4tLpi6hlIUrKg7hN6oZNz2LaRqJ-xlWQoqnX41D459M130_provenance.
- assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_provenance.
- NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.