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Author/Creator Senturk, Leyli

1. Clinical and molecular genetic findings of Crisponi/cold‐induced sweating syndrome (CS/CISS) spectrum in patients from Turkey. Issue 3 (12th July 2022)

Authors:
Yilmaz Gulec, Elif; Turgut, Gozde Tutku; Gezdirici, Alper; Karaman, Volkan; Ozturk, Fatma Nihal; Avci, Sahin; Kalayci, Tugba; Senturk, Leyli; Ayaz, Akif; Kayserili, Hulya; Uyguner, Zehra Oya; Altunoğlu, Umut
Journal:
Clinical genetics
Issue:
Volume 102:Issue 3(2022)
Page Start:
201
Record Type:
Journal Article
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2. Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients. Issue 1 (21st November 2017)

Authors:
Yilmaz, Rüstem; Szakszon, Katalin; Altmann, Anna; Altunoglu, Umut; Senturk, Leyli; McGuire, Marianne; Calabrese, Olga; Madan‐Khetarpal, Suneeta; Basel‐Vanagaite, Lina; Borck, Guntram
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 1(2018)
Page Start:
187
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Prenatal ultrasonographic features in Blomstrand osteochondrodysplasia: Antenatal case series confirmed by postmortem radiology and molecular diagnosis. (20th July 2022)

Authors:
Sarac Sivrikoz, Tugba; Kalayci, Tugba; Senturk, Leyli; Karaman, Volkan; Kalelioglu, Ibrahim Halil; Has, Recep; Kayserili, Hulya; Uyguner, Zehra Oya; Nishimura, Gen; Altunoglu, Umut
Journal:
Prenatal diagnosis
Issue:
Volume 42:Number 12(2022)
Page Start:
1503
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗