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Tulay Simsek

Showing results (21-30 of 24) with videos related to

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Acta Ophthalmologica|July 12, 2008
A new autosomal dominant Peters' anomaly phenotype expanding the anterior segment dysgenesis spectrumNilufer Berker, Yasemin Alanay, Ufuk Elgin, et al.
Hormone Research in Paediatrics|January 10, 2019
Clinical, Histochemical, and Molecular Study of Three Turkish Siblings Diagnosed with H Syndrome, and Literature ReviewEnver Simsek, Tulay Simsek, Makbule Eren, et al.
BMC Medical Genetics|June 20, 2018
SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case reportShoko Horita, Enver Simsek, Tulay Simsek, et al.
Molecular Vision|January 5, 2011
Novel mutations in the USH1C gene in Usher syndrome patientsMaría José Aparisi, Gema García-García, Teresa Jaijo, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Acta Ophthalmologica|July 12, 2008
A new autosomal dominant Peters' anomaly phenotype expanding the anterior segment dysgenesis spectrumNilufer Berker, Yasemin Alanay, Ufuk Elgin, et al.
Hormone Research in Paediatrics|January 10, 2019
Clinical, Histochemical, and Molecular Study of Three Turkish Siblings Diagnosed with H Syndrome, and Literature ReviewEnver Simsek, Tulay Simsek, Makbule Eren, et al.
BMC Medical Genetics|June 20, 2018
SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case reportShoko Horita, Enver Simsek, Tulay Simsek, et al.
Molecular Vision|January 5, 2011
Novel mutations in the USH1C gene in Usher syndrome patientsMaría José Aparisi, Gema García-García, Teresa Jaijo, et al.
Pageof 3