D. Gül

发表

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

F. Baş, F. Darendeliler, F. Demirel, 2016, American journal of medical genetics. Part A.

Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene

John E. Cockerham, L. Biesecker, J. Johnston, 2008, BMC Medical Genetics.

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

S. Poyrazoglu, F. Baş, F. Darendeliler, 2015, Journal of clinical research in pediatric endocrinology.

Rheumatic and Autoimmune Diseases May Have a Role in Disease Progression of Myelodysplastic Syndrome

Y. Terzi, D. Torun, C. Beyan, 2012 .

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

F. Baş, F. Darendeliler, F. Demirel, 2015, Journal of clinical research in pediatric endocrinology.

Turner Syndrome and Associated Problems in

F. Baş, F. Darendeliler, F. Demirel, 2015 .

Prenatal Diagnosis in a Family of TNFRSF11A (RANK) Gene Mutation Detection: A Case Report

M. Karkucak, T. Yakut, O. Gorukmez, 2014 .

Study of Autoimmunity in Klinefelter's Syndrome and Idiopathic Hypogonadotropic Hypogonadism

Z. Yeşilova, D. Gül, A. Inal, 2002, Journal of Clinical Immunology.

Analysis of the dermatoglyphics in Turkish patients with Klinefelter's syndrome

D. Gül, M. Solak, F. Çam, 2008 .

Unilateral proximal femoral focal deficiency and Hirschsprung disease.

D. Gül, H. Oztürk, 2000, Clinical dysmorphology.

Facial dysmorphism, multiple pigmented nevi, osteoporosis, brachydactyly, and other skeletal changes in a male: a new syndrome?

M. Sağlam, D. Gül, C. Oktenli, 2003, Clinical dysmorphology.

Application of the ‘Apt test’ in Prenatal Diagnosis to evaluate the Fetal Origin of Blood obtained by Cordocentesis: results of 30 pregnancies

G. Oǧur, D. Gül, M. Bahçe, 1997, Prenatal diagnosis.

Variable clinical expression of Holt-Oram syndrome in three generations.

G. Oǧur, D. Gül, M. Lenk, 1998, The Turkish journal of pediatrics.

Saethre-Chotzen Syndrome Presenting with Incomplete Renal Fanconi Syndrome

M. Sağlam, D. Gül, C. Oktenli, 2002, Nephron.

Acrocallosal syndrome: report of five Turkish patients.

D. Gül, H. Ulucan, R. Akın, 2004, Clinical Dysmorphology.

Adams-Oliver syndrome: further evidence for autosomal recessive inheritance.

D. Gül, R. Akın, E. Gökçay, 2001, Clinical dysmorphology.

Evidence for autosomal recessive inheritance of split hand/split foot malformation: a report of nine cases.

D. Gül, C. Oktenli, 2002, Clinical dysmorphology.

Digital Amputations Caused By Amniotic Bands a Case Report

D. Gül, D. Akyol, V. Baltacı, 1998 .

De novo pericentric inversion of chromosome 5 in a girl with mental retardation and unilateral ear malformation

D. Gül, H. Ulucan, R. Akın, 2006, American journal of medical genetics. Part A.

Severe Intrauterine Growth Retardation, Aged Facial Appearance, and Congenital Heart Disease in a Newborn with Johanson–Blizzard Syndrome

G. Oǧur, D. Gül, M. Lenk, 2000, Pediatric Cardiology.

Third case of WAGR syndrome with severe obesity and constitutional deletion of chromosome (11)(p12p14).

G. Oǧur, D. Gül, O. Ozcan, 2002, American journal of medical genetics.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

F. Atik, Z. Candemir, C. N. Semerci, 2004, Annales de genetique.

Woodhouse and Sakati syndrome (MIM 241080): report of a new patient.

Z. Odabaşı, H. Mergen, D. Gül, 2000, Clinical Dysmorphology.

Specific Polymorphisms of IL-1? Genes (-511, +3953) and Their Probable Effects on IL-1? Production in Idiopatic Hypogonadotropic Hypogonadism

M. Kutlu, E. Bolu, D. Gül, 2010 .

Caudothalamic groove cysts in Zellweger syndrome

T. Kendirli, D. Gül, B. Ünay, 2005, Clinical dysmorphology.

GAPO syndrome in three relatives in a Turkish kindred.

D. Gül, B. Şayli, 1993, American journal of medical genetics.

Ophthalmic findings in GAPO syndrome.

E. Kurt, D. Gül, B. Şayli, 1999, Japanese journal of ophthalmology.

IgA deficiency associated with growth hormone deficiency in a boy with short arm deletion of chromosome 18 (46,XY,18p-).

F. Gök, D. Gül, B. Şayli, 1994, Annales de genetique.

Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?

M. Sağlam, D. Gül, H. Ulucan, 2001, Clinical dysmorphology.

Goldenhar syndrome with duodenal atresia: a new finding.

D. Gül, B. Hacıhamdioğlu, S. Vurucu, 2008, Clinical dysmorphology.