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Systems Biology in Reproductive Medicine|July 4, 2023
A rare ring chromosome 21 abnormality is associated with azoospermia in two different phenotypically normal casesEzgi Gizem Berkay, Birsen Karaman, Seher Başaran
Molecular Syndromology|July 14, 2020
Three Offspring with Cri-du-Chat Syndrome from Phenotypically Normal ParentsDilek U Alkaya, Birsen Karaman, Beyhan Tüysüz
Prenatal Diagnosis|October 19, 2005
Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findingsHalil Aslan, Birsen Karaman, Gokhan Yildirim, et al.
The Turkish Journal of Pediatrics|March 9, 2021
A rare intrauterine onset growth retardation syndrome caused by mosaic 19p13.3 microduplication: evaluation of GH/IGF- 1 axis and GH therapy responseEmre Özer, Birsen Karaman, Nilay Güneş, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 16, 2018
Chromosome 14q11.2-q21.1 duplication: a rare cause of West syndromeÖzdem Ertürk Çetin, Cengiz Yalçınkaya, Birsen Karaman, et al.
Clinical Endocrinology|February 7, 2021
Growth and relationship of phenotypic characteristics with gonadal pathology and tumour risk in patients with 45, X/46, XY mosaicismSukran Poyrazoglu, Firdevs Bas, Birsen Karaman, et al.
F1000Research|June 25, 2019
Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disabilityMurat Kaya, İlknur Suer, Şükrü Öztürk, et al.
Scottish Medical Journal|July 21, 2022
Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13Murat Kaya, Ilknur Suer, Tugba Kalayci, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Gorlin-Chaudhry-Moss syndrome revisited: expanding the phenotypeRasim O Rosti, Kadri Karaer, Birsen Karaman, et al.
Turkish Archives of Pediatrics|March 17, 2025
Clinical and Molecular Analyses in 8 New Craniofrontonasal Syndrome Families: Revisiting the Mild End of the Phenotypic Spectrum in FemalesUmut Altunoglu, Birsen Karaman, Yasemin Alanay, et al.
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