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1 . Academic Journal
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey
저자
by
Kalb, S
;
Caglayan, A O
;
Degerliyurt, A
;
Schmid, S
;
Ceylaner, S
, et al.
소스
Clinical Genetics
. Jun 01, 2012 81(6):598-601
Web of Science
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7 . Academic Journal
AMNIOTIC-FLUID CELL-CULTURE AND SYRINGE TOXICITY: M21
저자
by
Ceylaner, G
;
Guven, M A
;
Ceylaner, S
;
Ekerbicer, H.
.
소스
Clinical Genetics
. Nov 01, 2010 78 Suppl 1:110-110
Web of Science
Scopus
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6 . Academic Journal
DISORDERS OF CONTIGUOUS GENES ARE NOT ALWAYS “CONTIGUOUS GENE SYNDROME”: LESSONS FROM A CASE WITH THREE DIFFERENT GENETIC DISORDERS: A90
저자
by
Aslan, D
;
Ceylaner, G
;
Ceylaner, S
.
소스
Clinical Genetics
. Nov 01, 2010 78 Suppl 1:40-41
Web of Science
Scopus
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5 . Academic Journal
THE MAJOR CAUSE OF TERMINAL TRANSVERSE LIMB DEFECT AND RELATED SYNDROMES IS THROMBOPHILIA. THE RESULTS OF PROSPECTIVE STUDY: A29
저자
by
Ceylaner, S
;
Ceylaner, G
;
Acar, K
;
Gül, D
;
Zencirlioglu, A
, et al.
소스
Clinical Genetics
. Nov 01, 2010 78 Suppl 1:24-24
Web of Science
Scopus
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7 .
Bir ailenin 16 üyesinde otozomal dominant kalıtım gösteren gelişimsel kalça çıkıgı
저자
by
Serdar Ceylaner
;
Muharrem Inan
;
Gülay Ceylaner
;
Fulya Ustunkan
;
Ceylaner, G.
, et al.
소스
Volume: 42, Issue: 4 289-291
Acta Orthopaedica et Traumatologica Turcica
Open Access (OpenAIRE)
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7 . Academic Journal
Postmortem evaluation of 220 prenatally diagnosed fetuses with neural tube defects: detection of associated anomalies in a Turkish population
저자
by
Ceylaner, S
;
Ceylaner, G
;
Gunyeli, I
;
Ekici, E
;
Tug, M
, et al.
소스
PRENATAL DIAGNOSIS
; FEB 2006, 26 2, p147-p153, 7p.
Scopus
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7 . Academic Journal
Prenatal diagnosis of Meckel Gruber syndrome presenting with renal agenesis: Report of a case
저자
by
Guven, MA
;
Ceylaner, S
;
Ceylaner, G
;
Gul, D
;
Ertas, IE
.
소스
GENETIC COUNSELING
; 2006, 17 1, p65-p68, 4p.
Scopus
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7 . Academic Journal
A novel mutation in the lysyl hydroxylase 1 gene causes decreased lysyl hydroxylase activity in an Ehlers-Danlos VIA patient
저자
by
Walker, LC
;
Overstreet, MA
;
Siddiqui, A
;
De Paepe, A
;
Ceylaner, G
, et al.
소스
JOURNAL OF INVESTIGATIVE DERMATOLOGY
; MAY 2005, 124 5, p914-p918, 5p.
Full Text (ScienceDirect)
Full Text (ScienceDirect O/A)
Scopus
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7 . Academic Journal
A case of fetal anticonvulsant syndrome with severe bilateral upper limb defect
저자
by
Guven, MA
;
Batukan, C
;
Ceylaner, S
;
Ceylaner, G
;
Uzel, M
.
소스
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE
; FEB 2006, 19 2, p115-p117, 3p.
Scopus
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7 . Academic Journal
Craniosynostosis and ectopia lentis in a propositus whose parents are cousins
저자
by
Guven, D
;
Kalayci, D
;
Hasiripi, H
;
Ceylaner, S
;
Ceylaner, G
.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
; APR 15 2005, 134A 2, p231-p231, 1p.
Scopus
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