Published in Int J Cancer on November 15, 1967
Abdominal Burkitt-type lymphomas in Algeria. Br J Cancer (1984) 0.82
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
The oculocerebrocutaneous (Delleman) syndrome. J Med Genet (1988) 0.94
A new polydactyly/imperforate-anus/vertebral-anomalies syndrome? Lancet (1968) 0.94
Familial translocation (3p 15p) with partial trisomy for the upper arm of chromosome 3 in two sibs. J Pediatr (1976) 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
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
Letter: Birth defects and oral contraceptives. Lancet (1973) 0.86
Familial Mediterranean fever and polyarteritis nodosa: experience of five paediatric cases. A causal relationship or coincidence? Eur J Pediatr (1997) 0.86
Partial deletion 21: case report with biochemical studies and review. J Med Genet (1987) 0.85
Additional evidence for a deleted gene for serum alpha-1-antitrypsin. N Engl J Med (1973) 0.84
3C syndrome: another case. Clin Genet (1989) 0.84
An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome? J Med Genet (1981) 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
Cytogenetic findings in acute monocytic leukemia in a renal allograft recipient. Cancer Genet Cytogenet (1986) 0.83
Familial deletion of chromosome 18 (p11.2). Ann Genet (1996) 0.83
Nitroblue tetrazolium test in children with malnutrition. J Pediatr (1972) 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
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
Coffin-Siris syndrome. Am J Dis Child (1978) 0.81
Goodpasture's syndrome (pulmonary hemosiderosis with nephritis). Clin Pediatr (Phila) (1976) 0.81
Cerebro-oculo-nasal syndrome: another case and review of the literature. Clin Dysmorphol (1998) 0.81
Chromosome aberration in ectopia cordis (46,XX,17q+) Am Heart J (1978) 0.81
An unusual chromosomal aberration in a case of Chediak-Higashi syndrome. J Med Genet (1970) 0.80
Trisomy-8 syndrome. Humangenetik (1974) 0.80
Corneal opacity, microphthalmia, mental retardation, microcephaly and generalized muscular spasticity associated with hyperglycinemia. Clin Genet (1974) 0.80
Thymic dysplasia associated with dyschondroplasia in an infant. Am J Dis Child (1972) 0.80
Immunological studies in ataxia-telangiectasia. Clin Genet (1974) 0.80
Partial trisomy 13q identified by sequential fluorescence in situ hybridization. Am J Med Genet (1995) 0.79
Induction of AGAMOUS gene expression plays a key role in ripening of tomato sepals in vitro. Plant Mol Biol (1998) 0.79
45,XO Turner's syndrome, Wilm's tumor and imprforate anus. Humangenetik (1971) 0.79
Sister chromatid exchange in lymphocytes of patients with cancer of the larynx. Am J Otolaryngol (1991) 0.79
Ankylosis, facial anomalies, and pulmonary hypoplasia syndrome. Am J Dis Child (1979) 0.79
The association between Henoch-Schönlein syndrome and renal amyloidosis: a proposal of a pathogenic mechanism. Turk J Pediatr (1994) 0.78
Hereditary congenital coxa vara with dominant inheritance? Humangenetik (1971) 0.78
Turner's and Stein-Leventhal's syndrome in two sisters. Turk J Pediatr (1971) 0.78
Intestinal mucosa in children with geophagia and iron-deficiency anaemia. Scand J Haematol (1970) 0.78
The Gordon syndrome. J Med Genet (1980) 0.78
The association of nephrotic syndrome and renal vein thrombosis: a clinicopathological analysis of eight pediatric patients. Turk J Pediatr (1990) 0.78
Hemolytic-uremic syndrome (HUS): a clinicopathological study of 15 cases. Turk J Pediatr (1993) 0.78
Prenatal studies in a family with transcobalamin II deficiency. Am J Hum Genet (1987) 0.77
Imperforate anus (polydactyly) vertebral anomalies syndrome: a hereditary trait? J Pediatr (1971) 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
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
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
Steroid treatment of soft-tissue tumors in Bannayan syndrome. Plast Reconstr Surg (1988) 0.76
Burkitt's lymphoma. (Studies of 20 cases seen in Hacettepe Children's Hospital compared with Burkitt's tumor in African children. Turk J Pediatr (1973) 0.76
Giemsa banding patterns of 13/14, 21/21 translocations, Philadelphia chromosome and trisomy 18. Turk J Pediatr (1972) 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
Pulmonary agenesis: importance of detailed cytogenetic studies. Am J Med Genet (1998) 0.75
Optic glioma of childhood: clinical, histopathological, and histochemical observations. Br J Ophthalmol (1989) 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
'Novel' immunodeficiency syndrome may be a previously described entity. Clin Genet (2000) 0.75
A condition resembling congenital hypoplastic anemia occurring in a mother and son. Clin Pediatr (Phila) (1982) 0.75
Jejunal mucosa in infantile malnutrition. Acta Paediatr Scand (1970) 0.75
Werner's syndrome. Turk J Pediatr (1971) 0.75
Genetic counseling: an integral component of primary medical care. J Okla State Med Assoc (1984) 0.75
Familial mental retardation with an incidental balanced t(12;16) translocation. South Med J (1981) 0.75
Fibrodysplasia ossificans progressiva presenting as fibrous scalp nodules. Cleve Clin Q (1984) 0.75
Bilateral ankylosed thumbs and mental retardation. Am J Med Genet (1990) 0.75
Laurence-Moon-Biedl syndrome in presumably identical twins. Humangenetik (1971) 0.75
Oculodentodigital dysplasia syndrome. Acta Paediatr Scand (1971) 0.75
Australia antigen in Turkey. Lancet (1971) 0.75
Split notochord syndrome with dorsal enteric fistula and sacral agenesis. Teratology (1988) 0.75
Fragile X-linked mental retardation: a new genetic entity. J Okla State Med Assoc (1982) 0.75
Recombinant DNA and the physician. J Okla State Med Assoc (1986) 0.75
A new syndrome of dysmorphogenesis: imperforate-anus associated with poly-oligodactyly and skeletal (mainly vertebral) anomalies. Acta Paediatr Scand (1971) 0.75
Cloverleaf skull associated with unusual skeletal anomalies. Pediatr Radiol (1987) 0.75
Skeletal dysplasia in an infant with hypertelorism, hypospadias, developmental delay, and a complex chromosomal translocation. South Med J (1987) 0.75
A panacea for all ills? Nurs Times (1991) 0.75
"Cat eye" syndrome with normal chromosomes. Lancet (1970) 0.75