Published in Lancet on June 02, 1973
Maternal serum free beta hCG screening: results of studies including 480 cases of Down syndrome. Prenat Diagn (1994) 2.17
Congenital aplasia of the thymus gland (DiGeorge's syndrome). N Engl J Med (1968) 1.49
Gonadal dysgenesis in a patient with an X;3 translocation: case report and review. J Med Genet (1980) 1.40
Dermatoglyphic findings in Laurence-Moon-Biedl syndrome. Lancet (1973) 1.38
Chronic neutropenia and abnormal cellular immunity in cartilage-hair hypoplasia. N Engl J Med (1970) 1.27
Spondylocostal dysplasia and neural tube defects. J Med Genet (1991) 1.26
Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndrome. J Pediatr (1973) 1.20
Contribution of fetal/maternal incompatibility to aetiology of pre-eclamptic toxaemia. Lancet (1971) 1.16
Agenesis of the lung associated with a chromosome abnormality (46,XX,2p+). J Med Genet (1980) 1.09
Polydactyly with triphalangeal thumbs, brachydactyly, camptodactyly, congenital dislocation of the patellas, short stature and borderline intelligence. Birth Defects Orig Artic Ser (1976) 1.09
Hereditary defect of the sacrum. Humangenetik (1975) 1.07
Microcephaly, short stature, and developmental delay associated with a chemotactic defect and transient hypogammaglobulinaemia in two brothers. J Med Genet (1986) 1.07
Pattern profile analysis of the hand in trichlorhinophalangeal syndrome. Pediatrics (1977) 1.04
Aspects of pre-eclamptic toxaemia of pregnancy, consanguinity, twinning in Ankara. J Med Genet (1976) 1.03
Association of birth defects and immunodeficiency. J Pediatr (1979) 1.01
A homozygote for pericentric inversion of chromosome 4. J Med Genet (1982) 0.99
Geophagia associated with iron-deficiency anemia, hepatosplenomegaly, hypogonadism and dwarfism. A syndrome probably associated with zinc deficiency. Clin Pediatr (Phila) (1969) 0.98
Community genetics. I. J Okla State Med Assoc (1975) 0.98
Incidence and distribution of hepatitis Bs-antigen in Turkey. Vox Sang (1976) 0.96
The oculocerebrocutaneous (Delleman) syndrome. J Med Genet (1988) 0.94
Familial translocation (3p 15p) with partial trisomy for the upper arm of chromosome 3 in two sibs. J Pediatr (1976) 0.94
A new polydactyly/imperforate-anus/vertebral-anomalies syndrome? Lancet (1968) 0.94
Cervico-ocula-acusticus syndrome of Wildervanck. Case report. Turk J Pediatr (1973) 0.92
Immunodeficiency in children with severe craniofacial anomalies. South Med J (1982) 0.92
Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin. Am J Dis Child (1982) 0.91
Mental retardation with blepharophimosis. J Med Genet (1987) 0.90
Juvenile rheumatoid arthritis: cervical spine involvement and MRI in early diagnosis. Turk J Pediatr (1996) 0.90
Phototherapy in nonobstructive, nonhemolytic jaundice. Pediatrics (1973) 0.88
Robinow syndrome: with special emphasis on dermatoglyphics and hand malformations (split hand). Clin Dysmorphol (1993) 0.87
Platelet survival in childhood idiopathic thrombocytopenic purpura in remission. J Pediatr (1976) 0.87
Letter: Birth defects and oral contraceptives. Lancet (1973) 0.86
Partial deletion 21: case report with biochemical studies and review. J Med Genet (1987) 0.85
An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome? J Med Genet (1981) 0.84
3C syndrome: another case. Clin Genet (1989) 0.84
Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 case. Am J Med Genet (1998) 0.84
Additional evidence for a deleted gene for serum alpha-1-antitrypsin. N Engl J Med (1973) 0.84
Familial deletion of chromosome 18 (p11.2). Ann Genet (1996) 0.83
Usefulness of pulse-wave Doppler tissue sampling and dobutamine stress echocardiography for identification of false positive inferior wall defects in SPECT. Jpn Heart J (2000) 0.83
Cytogenetic findings in acute monocytic leukemia in a renal allograft recipient. Cancer Genet Cytogenet (1986) 0.83
Nitroblue tetrazolium test in children with malnutrition. J Pediatr (1972) 0.83
Familial trigonocephaly associated with short stature and developmental delay. Am J Dis Child (1981) 0.82
Sensorineural hearing loss and enamel hypoplasia with subtle nail findings: another family with Heimler's syndrome. Clin Dysmorphol (2003) 0.82
Detection of a familial cryptic translocation by fluorescent in situ hybridisation. J Med Genet (1996) 0.82
Hemolysis and jaundice in the newborn following maternal treatment with sulfamethoxypyridazine (kynex). Pediatrics (1965) 0.81
Cerebro-oculo-nasal syndrome: another case and review of the literature. Clin Dysmorphol (1998) 0.81
Coffin-Siris syndrome. Am J Dis Child (1978) 0.81
Goodpasture's syndrome (pulmonary hemosiderosis with nephritis). Clin Pediatr (Phila) (1976) 0.81
Chromosome aberration in ectopia cordis (46,XX,17q+) Am Heart J (1978) 0.81
Nutrition, immunity and infections: T lymphocyte subpopulations in protein--energy malnutrition. J Trop Pediatr (1993) 0.81
Trisomy-8 syndrome. Humangenetik (1974) 0.80
Thymic dysplasia associated with dyschondroplasia in an infant. Am J Dis Child (1972) 0.80
Corneal opacity, microphthalmia, mental retardation, microcephaly and generalized muscular spasticity associated with hyperglycinemia. Clin Genet (1974) 0.80
Immunological studies in ataxia-telangiectasia. Clin Genet (1974) 0.80
Epidemiological aspects of childhood poisonings in Ankara: a 10-year survey. Hum Toxicol (1987) 0.80
An unusual chromosomal aberration in a case of Chediak-Higashi syndrome. J Med Genet (1970) 0.80
Induction of AGAMOUS gene expression plays a key role in ripening of tomato sepals in vitro. Plant Mol Biol (1998) 0.79
The importance of pulmonary function tests in adenotonsillectomy indications. Indian J Pediatr (1994) 0.79
45,XO Turner's syndrome, Wilm's tumor and imprforate anus. Humangenetik (1971) 0.79
Cytosine arabinoside (NSC-63878) in acute leukemia in children. Cancer Chemother Rep (1966) 0.79
Combined chemotherapy in 76 children with non-Hodgkin's lymphoma excluding Burkitt's lymphoma. Br J Cancer (1987) 0.79
Ankylosis, facial anomalies, and pulmonary hypoplasia syndrome. Am J Dis Child (1979) 0.79
Partial trisomy 13q identified by sequential fluorescence in situ hybridization. Am J Med Genet (1995) 0.79
Turner's and Stein-Leventhal's syndrome in two sisters. Turk J Pediatr (1971) 0.78
Hereditary congenital coxa vara with dominant inheritance? Humangenetik (1971) 0.78
The Gordon syndrome. J Med Genet (1980) 0.78
Intestinal mucosa in children with geophagia and iron-deficiency anaemia. Scand J Haematol (1970) 0.78
Paediatric endobronchial leiomyoma mimicking asthma. Respir Med (1995) 0.78
Prenatal studies in a family with transcobalamin II deficiency. Am J Hum Genet (1987) 0.77
13-15 (D1) trisomy syndrome. (With special emphasis on pathological findings). Turk J Pediatr (1971) 0.77
The radial dysplasia/imperforate anus/vertebral anomalies syndrome (the VATER association): Developmental aspects and eye findings. Acta Paediatr Scand (1977) 0.77
A case of lymphosarcoma, resembling Burkitt's tumor, in a Turkish child. Int J Cancer (1967) 0.77
Trial of a new pain assessment tool in patients with low education: the full cup test. Int J Clin Pract (2007) 0.77
Imperforate anus (polydactyly) vertebral anomalies syndrome: a hereditary trait? J Pediatr (1971) 0.77
The response of the myocardial metabolism to atrial pacing in patients with coronary slow flow. Int J Cardiol (2001) 0.77
Unusual calcium deposition in cartilage associated with short stature and peculiar facial features: a case report. Pediatr Radiol (1973) 0.76
Giemsa banding patterns of 13/14, 21/21 translocations, Philadelphia chromosome and trisomy 18. Turk J Pediatr (1972) 0.76
Steroid treatment of soft-tissue tumors in Bannayan syndrome. Plast Reconstr Surg (1988) 0.76
CD1+ cells in mothers of stillborn infants with neural tube defects. Am J Med Genet (1995) 0.75
Letter: Misuse of acronyms and the VATER association. J Pediatr (1975) 0.75
The incidence of PTC taste sensitivity in the population of Ankara. Turk J Pediatr (1966) 0.75
The heritability of liability to congenital dislocation of the hip. Turk J Pediatr (1972) 0.75
Pulmonary agenesis: importance of detailed cytogenetic studies. Am J Med Genet (1998) 0.75
'Novel' immunodeficiency syndrome may be a previously described entity. Clin Genet (2000) 0.75
Case report. The cat-eye syndrome with unusual skeletal malformations. Acta Paediatr Scand (1974) 0.75
Plasma, erythrocyte, and leukocyte ascorbic acid concentrations in children with iron deficiency anemia. J Pediatr (1975) 0.75
Anterior sacral meningocele. JAMA (1977) 0.75
Posterior fossa pseudotumour due to viral encephalitis in a child. Pediatr Radiol (1997) 0.75
Urinary nitrite excretion in low birth weight neonates with systemic inflammatory response syndrome. Biol Neonate (1997) 0.75
Ascorbic acid status in children with malnutrition. Turk J Pediatr (1974) 0.75
Pancreatic changes associated with cases of thymic dysplasia. Turk J Pediatr (1977) 0.75
Dermatoglyphic findings in familial coxa vara with dominant inheritance. Turk J Pediatr (1974) 0.75
Congenital contractural arachnodactyle. Turk J Pediatr (1974) 0.75
Frequency of red cell adenosine deaminase and 6-phosphogluconate dehydrogenase in a sample of the Turkish population. Hum Hered (1974) 0.75
Letter: Sacral agenesis. Pediatrics (1975) 0.75
A case of common truncus arteriosus with rare cardiac abnormalities. Turk J Pediatr (1994) 0.75
Isoimmunization and hemolytic transfusion reaction due to anti-c and anti-Jk combination. Turk J Pediatr (1979) 0.75
Chromosome variants in children with psychiatric disorders. Am J Psychiatry (1977) 0.75
Effect of exchange transfusion on elimination of antibiotics in premature infants. Turk J Pediatr (1994) 0.75
Breast milk versus infant formulas: effects on intestinal blood flow in neonates. Indian J Pediatr (1995) 0.75
A new dominantly inherited syndrome of cleft palate. Humangenetik (1975) 0.75