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Clinical Genetics|November 1, 1995
A new syndrome with cardiac malformation, cleft lip-palate, microcephaly and digital anomalies?E F Perçin, F Düzcan, G Kafali, et al.
Genetic Counseling (Geneva, Switzerland)|September 12, 2018
THE 3rd W522X MUTATION IN EIF2AK3 GENE FROM TURKEY: A NEW PATIENT WITH WOLCOTT-RALLISON SYNDROMET Bahsi, A Unal, A Bakir, et al.
Genetic Counseling (Geneva, Switzerland)|September 12, 2018
MATTHEW-WOOD SYNDROME: A CASE WITH DEXTROCARDIA AND STREAK GONADSP Ozyavuz Cubuk, L Ho, B Reversade, et al.
Genetic Counseling (Geneva, Switzerland)|November 21, 2007
A new case of hairy elbows syndrome (hypertrichosis cubiti)A Koç, K Karaer, M A Ergün, et al.
Genetic Counseling (Geneva, Switzerland)|September 12, 2018
SUBMICROSCOPIC DUPLICATION OF 8q24.3 REGION IS A POTENTIAL CANDIDATE FOR DISORDERS OF SEX DEVELOPMENTF N Dilek, E F Perçin, H Kayserili, et al.
Genetic Counseling (Geneva, Switzerland)|November 11, 2008
Dubowitz syndrome: a cholesterol metabolism disorder?E Yeşilkaya, K Karaer, A Bideci, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
A case with bilateral radio-ulnar synostosisA Koç, A O Kaymak, K Karaer, et al.
Genetic Counseling (Geneva, Switzerland)|February 22, 2008
A boy with small supernumerary marker chromosome X identified by FISHA Koç, M Yirmibeş Karaoğuz, E Pala, et al.
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