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    Results: 1 to 20 of 73

    1.

    A 19-year follow-up of a patient with type 3 ectrodactyly-ectodermal dysplasia-clefting syndrome who developed non-Hodgkin lymphoma.

    Balci S, Engiz O, Otken G, Sipahier M, Gursu G, Kandemir B.

    Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 Sep;108(3):e91-5.PMID: 19716498 [PubMed - in process]Related articles

    2.

    ALX4 dysfunction disrupts craniofacial and epidermal development.

    Kayserili H, Uz E, Niessen C, Vargel I, Alanay Y, Tuncbilek G, Yigit G, Uyguner O, Candan S, Okur H, Kaygin S, Balci S, Mavili E, Alikasifoglu M, Haase I, Wollnik B, Akarsu NA.

    Hum Mol Genet. 2009 Nov 15;18(22):4357-66. Epub 2009 Aug 19.PMID: 19692347 [PubMed - in process]Related articles

    3.

    A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).

    Balci S, Aypar E, Beksaç MS, Bartsch O.

    Genet Couns. 2009;20(2):125-32.PMID: 19650409 [PubMed - indexed for MEDLINE]Related articles

    4.

    A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome.

    Balci S, Güçer S, Orhan D, Karagöz T.

    Turk J Pediatr. 2008 Nov-Dec;50(6):595-9.PMID: 19227428 [PubMed - indexed for MEDLINE]Related articles

    5.

    Limb anomalies and anemia: Aase-Smith syndrome.

    Balci S.

    Fetal Pediatr Pathol. 2008;27(6):292-3. No abstract available. PMID: 19065327 [PubMed - indexed for MEDLINE]Related articles

    6.

    Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue.

    Orhan D, Balci S, Deren O, Utine EG, Başaran A, Kale G.

    Turk J Pediatr. 2008 Jul-Aug;50(4):395-9.PMID: 19014058 [PubMed - indexed for MEDLINE]Related articles

    7.

    Approach in an adolescent Proteus male patient with megafoot.

    Derman O, Balci S, Engiz O.

    Turk J Pediatr. 2008 Mar-Apr;50(2):200-3.PMID: 18664091 [PubMed - indexed for MEDLINE]Related articles

    8.

    A new case of VACTERL association with congenital arachnoid cyst.

    Unal S, Kibar AE, Ozaydin E, Karadag N, Balci S.

    Clin Dysmorphol. 2008 Jul;17(3):221-2. No abstract available. PMID: 18541975 [PubMed - indexed for MEDLINE]Related articles

    9.

    31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): clinical, neuroradiologic, audiologic and cytogenetic findings.

    Engiz O, Balci S, Unsal M, Ozer S, Oguz KK, Aktas D.

    Genet Couns. 2007;18(3):277-88.PMID: 18019368 [PubMed - indexed for MEDLINE]Related articles

    10.

    Omentectomy for gynecologic cancer: how much sampling is adequate for microscopic examination?

    Usubütün A, Ozseker HS, Himmetoglu C, Balci S, Ayhan A.

    Arch Pathol Lab Med. 2007 Oct;131(10):1578-81.PMID: 17922596 [PubMed - indexed for MEDLINE]Related articles

    11.

    Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome.

    Frank V, Ortiz Brüchle N, Mager S, Frints SG, Bohring A, du Bois G, Debatin I, Seidel H, Senderek J, Besbas N, Todt U, Kubisch C, Grimm T, Teksen F, Balci S, Zerres K, Bergmann C.

    Hum Mutat. 2007 Jun;28(6):638-9.PMID: 17437276 [PubMed - indexed for MEDLINE]Related articles

    12.

    Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3).

    Balci S, Unal A, Engiz O, Aktas D, Liehr T, Gross M, Mrasek K, Saygi S.

    Dev Med Child Neurol. 2007 Mar;49(3):219-24.PMID: 17355480 [PubMed - indexed for MEDLINE]Related articles

    13.

    Situs inversus totalis, renal and pancreatic dysplasia, and cysts as an autosomal recessive new entity?

    Balci S.

    Genet Med. 2007 Feb;9(2):137; author reply 137. No abstract available. PMID: 17304058 [PubMed - indexed for MEDLINE]Related articles

    14.

    Effective treatment of multifocal aggressive fibromatosis with low-dose chemotherapy.

    Caglar K, Ozyönüm H, Akalin M, Balci S.

    Turk J Pediatr. 2006 Oct-Dec;48(4):365-8.PMID: 17290575 [PubMed - indexed for MEDLINE]Related articles

    15.

    A 13-year-old female with Turner syndrome and achalasia.

    Balci S, Akcan AB, Senocak ME, Ciftçi AO, Ozaltin F.

    Turk J Pediatr. 2006 Jul-Sep;48(3):272-4.PMID: 17172077 [PubMed - indexed for MEDLINE]Related articles

    16.

    Bannayan-riley-ruvalcaba syndrome from the point of view of the pediatric surgeon.

    Ekinci S, Karnak I, Balci S, Tanyel FC, Büyükpamukçu N.

    Eur J Pediatr Surg. 2006 Jun;16(3):209-13.PMID: 16909363 [PubMed - indexed for MEDLINE]Related articles

    17.

    Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies.

    Balci S, Engiz O, Aktaş D, Vargel I, Beksaç MS, Mrasek K, Vermeesch J, Liehr T.

    Am J Med Genet A. 2006 Mar 15;140(6):628-32.PMID: 16470698 [PubMed - indexed for MEDLINE]Related articles

    18.

    A new case of omphalocele with absence of thumb.

    Balci S, Leblebicioğlu G, Yiğitkanli I.

    Turk J Pediatr. 2005 Jan-Mar;47(1):95-7. Review.PMID: 15884640 [PubMed - indexed for MEDLINE]Related articles

    19.

    Temporary dysplastic hematological features due to iron deficiency in a case of Poland syndrome.

    Aslan D, Balci S.

    Pediatr Hematol Oncol. 2004 Dec;21(8):711-5.PMID: 15739626 [PubMed - indexed for MEDLINE]Related articles

    20.

    Megalocornea-mental retardation (MMR or Neuhauser) syndrome: another case associated with cerebral cortical atrophy and Bifid uvula.

    Derbent M, Oto S, Alehan F, Ozçay F, Kinik S, Cetin I, Balci S.

    Genet Couns. 2004;15(4):477-80. No abstract available. PMID: 15658626 [PubMed - indexed for MEDLINE]Related articles

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