Matches in Nanopublications for { ?s ?p "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_assertion description "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_provenance.
- NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_assertion description "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- assertion description "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP284659.RA8V_t59mVrRXBCndxU4k8_kXWj1uR6oB8NXoWKjI3Wao130_assertion description "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284659.RA8V_t59mVrRXBCndxU4k8_kXWj1uR6oB8NXoWKjI3Wao130_provenance.
- NP284658.RASjjN92T5QktDQcPkWYLzylCxhpKCKLAvHE-_e3GWh4w130_assertion description "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284658.RASjjN92T5QktDQcPkWYLzylCxhpKCKLAvHE-_e3GWh4w130_provenance.