Published in Eur J Obstet Gynecol Reprod Biol on April 01, 1995
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Dermatoglyphic findings in Laurence-Moon-Biedl syndrome. Lancet (1973) 1.38
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Homozygous and compound heterozygous mutations at the Werner syndrome locus. Hum Mol Genet (1996) 1.19
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Dermatological manifestations of 71 Down syndrome children admitted to a clinical genetics unit. Clin Genet (1996) 0.96
31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): clinical, neuroradiologic, audiologic and cytogenetic findings. Genet Couns (2007) 0.95
Thoracoschisis associated with diaphragmatic hernia in a 31-week-old stillbirth. Turk J Pediatr (2001) 0.94
Serosurveillance study on transmission of H5N1 virus during a 2006 avian influenza epidemic. Epidemiol Infect (2010) 0.94
True hermaphroditism: clinical features, genetic variants and gonadal histology. J Pediatr Endocrinol Metab (2001) 0.93
Cervico-ocula-acusticus syndrome of Wildervanck. Case report. Turk J Pediatr (1973) 0.92
Familial selective vitamin B12 malabsorption (Imerslund-Gräsbeck syndrome) in a pool of Turkish patients. Pediatr Hematol Oncol (1995) 0.91
Serum bactericidal and opsonic activities in patients with non-alcoholic cirrhosis. Q J Med (1985) 0.89
Immunological: reactions involving leukocytes: III. Agranulocytosis induced by antithyroid drugs. Johns Hopkins Med J (1976) 0.88
Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome. Genet Couns (2004) 0.87
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Cleidooccipital muscle: an anomalous muscle in the neck region. Folia Morphol (Warsz) (2001) 0.86
The endocrinological evaluation of bilateral and unilateral oophorectomy in premenopausal women. Int J Fertil (1983) 0.86
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An atypical form of dyskeratosis congenita with renal agenesis and no mutation in DKC1, TERC and TERT genes. J Eur Acad Dermatol Venereol (2009) 0.85
Familial selective vitamin B12 malabsorption in three families. Turk J Pediatr (1980) 0.85
Germ cell tumours in a brother and sister. Acta Paediatr (1997) 0.84
Can cytomegalovirus cause brachydactyly? A case report and review of the literature. Clin Genet (1993) 0.83
Acute effect of low-flux hemodialysis process on the results of the interferon-gamma-based QuantiFERON-TB Gold In-Tube test in end-stage renal disease patients. Transpl Infect Dis (2008) 0.83
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An intelligent diagnostic system for the assessment of gestational age based on ultrasonic fetal head measurements. Technol Health Care (1996) 0.82
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A male case with double aneuploidy (48,XXY,+21). Genet Couns (2008) 0.82
Vasculogenesis in early human placental villi: an ultrastructural study. Ann Anat (1999) 0.81
Uterus retrieval in cadaver: technical aspects. Clin Exp Obstet Gynecol (2014) 0.81
An unusual chromosomal aberration in a case of Chediak-Higashi syndrome. J Med Genet (1970) 0.80
Triphalangeal thumb in a case of VACTERL-hydrocephalus association. Genet Couns (2003) 0.80
Type 1 sirenomelia in one of male twins, with imperforate anus in the other male twin. Clin Dysmorphol (2000) 0.80
Fetal hemoglobin in various forms of childhood leukemia. Relation to relapse and remission. Clin Pediatr (Phila) (1970) 0.80
Corneal opacity, microphthalmia, mental retardation, microcephaly and generalized muscular spasticity associated with hyperglycinemia. Clin Genet (1974) 0.80
An artificial intelligent diagnostic system on differential recognition of hematopoietic cells from microscopic images. Cytometry (1997) 0.80
Tibial tubercle position and patellar height as indicators of malalignment in women with anterior knee pain. Clin Anat (2000) 0.80
Serum bactericidal and opsonic activities in chronic lymphocytic leukemia and multiple myeloma. Am J Hematol (1986) 0.79
45,XO Turner's syndrome, Wilm's tumor and imprforate anus. Humangenetik (1971) 0.79
Sirenomelia in an infant of a diabetic mother. A case report. Turk J Pediatr (1996) 0.79
Ultrasonographic detection of single umbilical artery: a simple marker of fetal anomaly. Int J Gynaecol Obstet (1997) 0.79
Two brothers with hypospadias, hypertelorism, upper lid coloboma and mixed type hearing loss: a new syndrome. Clin Genet (1998) 0.79
Vitamin A supplementation in acute diarrhea. J Pediatr Gastroenterol Nutr (2000) 0.79
An expert diagnostic system based on neural networks and image analysis techniques in the field of automated cytogenetics. Technol Health Care (1996) 0.78
Free microvascular transfer of the vermiform appendix for creation of a tracheo-oesophageal fistula: A new method of voice reconstruction. J Plast Reconstr Aesthet Surg (2006) 0.78
Selective cerebral perfusion with aortic cannulation and short-term hypothermic circulatory arrest in aortic arch reconstruction. Perfusion (2013) 0.78
Familial microtia with meatal atresia in father and son. Turk J Pediatr (1974) 0.78
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Myeloperoxidase activity and bactericidal function of PMN in iron deficiency. Acta Haematol (1979) 0.78
Familial intestinal polyatresia syndrome. Clin Genet (1995) 0.78
Hyperhydroxyprolinaemia detected in newborn screening with tandem mass spectrometry. J Inherit Metab Dis (2004) 0.77
Middle and inner ear anomalies in a patient with CHARGE association. Genet Couns (2003) 0.77
Imperforate anus (polydactyly) vertebral anomalies syndrome: a hereditary trait? J Pediatr (1971) 0.77
Arterialized venous dorsal digital island flap for fingertip reconstruction. Plast Reconstr Surg (1998) 0.77
Cri-du-chat syndrome associated with arachnoid cyst causing triventricular hydrocephalus. Clin Dysmorphol (2001) 0.77
Serum vitamin B12 concentrations in children. Turk J Pediatr (1986) 0.77
Endoglin (CD 105) expression in human lymphoid organs and placenta. Ann Anat (1998) 0.77
13-15 (D1) trisomy syndrome. (With special emphasis on pathological findings). Turk J Pediatr (1971) 0.77
Unusual calcium deposition in cartilage associated with short stature and peculiar facial features: a case report. Pediatr Radiol (1973) 0.76
Bannayan-riley-ruvalcaba syndrome from the point of view of the pediatric surgeon. Eur J Pediatr Surg (2006) 0.76
Impaired glucose tolerance in pulmonary tuberculosis. Eur J Respir Dis (1987) 0.76
A Turkish family with Ellis-van Creveld syndrome in six siblings; linkage analysis on 4p16 region (D4S3360-D4S2366). Genet Couns (2008) 0.75
Measurement of nasal mucociliary activity in man with 99mTc-labelled resin particles. Arch Otorhinolaryngol (1984) 0.75
Diploid-triploid and tetraploid mosaicism in a child with cryptogenic cirrhosis and membranous glomerulonephritis: a causal relationship or coincidental association? Turk J Pediatr (1998) 0.75
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I. Turk J Pediatr (1994) 0.75
Multiple agminated Spitz nevi of the scalp. Ann Plast Surg (1999) 0.75
A case with multiple anomalies in the upper limb. Surg Radiol Anat (2001) 0.75
Classical phenylketonuria associated with Goldenhar's syndrome. A case report. Turk J Pediatr (1994) 0.75
Caval backflow: a potential problem during blood sampling from the hepatic vein. Metabolism (2001) 0.75
Absence of a hand (acheiria) in a child whose father was treated with cyclophosphamide for Behçet's disease. Turk J Pediatr (1984) 0.75
Gated myocardial perfusion scintigraphy in children with sickle cell anemia: correlation with echocardiography. Rev Esp Med Nucl (2011) 0.75
Outcome of kidney transplantation following end-stage renal disease due to reflux nephropathy. Transplant Proc (2011) 0.75
Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation. Genet Couns (2011) 0.75
[Clinical, radiological and anatomic analysis of 100 cases of operated herniated lumbar disks]. Union Med Can (1973) 0.75
Lethal chondrodysplasia punctata in two siblings. Turk J Pediatr (1988) 0.75
Potter's syndrome: bilateral renal agenesis (a report of two cases emphasizing associated malformations). Turk J Pediatr (1984) 0.75
Intussusception due to inflammatory fibroid polyp of the ileum. A report of two cases from Turkiye. Hiroshima J Med Sci (1995) 0.75
Isolated hepatic tuberculous abscess in a renal transplant recipient. Transplant Proc (2006) 0.75
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[Total knee prosthesis]. Union Med Can (1977) 0.75
[Acute glomerulonephritis in a pediatric unit]. Turk Hemsire Derg (1983) 0.75
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Co-occurrence of familial Mediterranean fever (FMF) heterozygote mutation and nail-patella syndrome (NPS) in 3 members of a family with LMX1B mutation analysis. Genet Couns (2007) 0.75
A large inguinal hernia with undescended testes and micropenis in Robinow syndrome. Clin Dysmorphol (1996) 0.75
Aase-Smith syndrome: report of a new case with unusual features. Turk J Pediatr (1994) 0.75
A new flap model in the rat: the pectoral skin flap. Ann Plast Surg (1999) 0.75
A new technique for substernal colon transposition with a breast dissector: report of 39 cases. J Plast Reconstr Aesthet Surg (2006) 0.75
[Leg amputation and immediate prosthetic fitting on the operating table]. Union Med Can (1973) 0.75
[Biomechanics of the knee]. Union Med Can (1980) 0.75
Leukemias associated with neurofibromatosis in children. Turk J Pediatr (1989) 0.75
Three cases of oblique facial cleft: etiology, tomographic evaluation and reconstruction. Clin Dysmorphol (1992) 0.75