Published in Hum Genet on May 10, 1977
Aberrant melanoblast migration associated with trisomy 18 mosaicism. J Med Genet (1983) 1.12
Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child. J Med Genet (1997) 0.77
Risk factors for anastomotic leakage after resection of rectal cancer. Br J Surg (1998) 3.45
Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry (2008) 2.07
[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]. C R Acad Sci Hebd Seances Acad Sci D (1973) 1.89
A multicentre, randomised phase II study of weekly or 3-weekly docetaxel in patients with metastatic breast cancer. Ann Oncol (2004) 1.85
Intersphincteric resection with excision of internal anal sphincter for conservative treatment of very low rectal cancer. Dis Colon Rectum (1999) 1.83
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. Am J Hum Genet (2000) 1.68
Congenital cutaneous defects as complications in surviving co-twins. Aplasia cutis congenita and neonatal volkmann ischemic contracture of the forearm. Arch Dermatol (1998) 1.67
A strategy for optimizing the monodispersity of fusion proteins: application to purification of recombinant HPV E6 oncoprotein. Protein Eng (2001) 1.59
Risk analysis of leukaemia incidence among people living along the Techa River: a nested case-control study. J Radiol Prot (2006) 1.54
[Acupuncture worth trying in severe tinnitus]. Lakartidningen (1998) 1.50
Schizencephaly: clinical and imaging features in 30 infantile cases. Brain Dev (2000) 1.43
Pericentric inversion and partial monosomy 4q associated with congenital anomalies. Hum Genet (1977) 1.42
[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)]. Cytogenet Cell Genet (1973) 1.40
Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p. Hum Genet (1978) 1.40
[Coffin-Lowry syndrome and hyperprolinemia]. Arch Fr Pediatr (1994) 1.40
[Children arthropod bites protective measures: insecticides and repellents]. Arch Pediatr (2007) 1.39
A somatic origin of homologous Robertsonian translocations and isochromosomes. Am J Hum Genet (1994) 1.31
Loop ileostomy versus loop colostomy for defunctioning low anastomoses during rectal cancer surgery. World J Surg (2001) 1.30
Formation of soluble inclusion bodies by hpv e6 oncoprotein fused to maltose-binding protein. Protein Expr Purif (2001) 1.29
Characterization of a selective and potent antagonist of human P2X(7) receptors, AZ11645373. Br J Pharmacol (2006) 1.29
An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature. Hum Genet (1990) 1.28
In-vitro activity of erythromycin, roxithromycin and CP 62993 against common paediatric pathogens. J Antimicrob Chemother (1987) 1.26
Control of myogenesis in the mouse myogenic C2 cell line by medium composition and by insulin: characterization of permissive and inducible C2 myoblasts. Differentiation (1988) 1.22
Liver resection of colorectal metastases in elderly patients. Br J Surg (2010) 1.21
The oncological safety of laparoscopic total mesorectal excision with sphincter preservation for rectal carcinoma. Surg Endosc (2005) 1.17
Second-generation three-dimensional reconstruction for rotational three-dimensional angiography. Acad Radiol (1998) 1.17
[Four new cases of X-autosome translocation in man (author's transl)]. Humangenetik (1975) 1.17
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy. Hum Mol Genet (1992) 1.14
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE. Transl Psychiatry (2012) 1.08
[Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"]. Ann Genet (1966) 1.07
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family. Hum Mol Genet (1994) 1.07
Adult human masseter muscle fibers express myosin isozymes characteristic of development. Muscle Nerve (1988) 1.06
Evaluation of certain food additives and contaminants. World Health Organ Tech Rep Ser (2007) 1.06
Exploring multifunctional agriculture. A review of conceptual approaches and prospects for an integrative transitional framework. J Environ Manage (2009) 1.06
Hyaluronan and healing of tympanic membrane perforations. An experimental study. Acta Otolaryngol Suppl (1987) 1.04
A novel microsatellite DNA marker at locus D7S1870 detects hemizygosity in 75% of patients with Williams syndrome. Am J Hum Genet (1995) 1.04
Phenotypic variability in van der Woude syndrome. Genet Couns (1995) 1.03
Correlates of intake of folic acid-containing supplements among pregnant women. Am J Obstet Gynecol (2006) 1.02
Estimated dietary exposure to principal food mycotoxins from the first French Total Diet Study. Food Addit Contam (2005) 1.01
Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder. Mol Psychiatry (2004) 1.01
Human exposure and internal dose assessments of acrylamide in food. Food Chem Toxicol (2005) 1.01
Novel P2X7 receptor antagonists. Bioorg Med Chem Lett (2003) 1.00
Chernobyl, 10 years after: health consequences. Epidemiol Rev (1997) 1.00
Hepatic undifferentiated embryonal sarcoma: malignant evolution of mesenchymal hamartoma? Study of one case with immunohistochemical and flow cytometric emphasis. J Hepatol (2001) 1.00
Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Mol Psychiatry (2009) 0.99
[Application of the controlled denaturation method: denaturation of previously stained preparations]. Ann Genet (1972) 0.98
Multicenter linkage study of schizophrenia loci on chromosome 22q. Mol Psychiatry (2004) 0.98
Assessment of intake from the diet. Food Chem Toxicol (2002) 0.98
[Bilateral anophthalmos. Facial anomalies and t(4;14) translocation]. J Genet Hum (1974) 0.98
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases. Ann Neurol (2000) 0.98
[Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)]. Ann Genet (1979) 0.98
Red cells life span, splenic sequestration and transfusion requirements in chronic renal failure treated by hemodialysis. Effects of bilateral nephrectomy. Clin Nephrol (1974) 0.98
Positive predictive value of the Xpert MRSA assay diagnostic for universal patient screening at hospital admission: influence of the local ecology. Eur J Clin Microbiol Infect Dis (2011) 0.97
Linkage disequilibrium on the COMT gene in French schizophrenics and controls. Am J Med Genet (1999) 0.97
[A second example of telomeric fusion 2 X chromosomes]. Ann Genet (1975) 0.97
Emergence and dissemination of multidrug resistant clones of Pseudomonas aeruginosa producing VIM-2 metallo-beta-lactamase in Belgium. Euro Surveill (2007) 0.96
Private function? Nurs Times (1994) 0.96
Cross-linked hyaluronan (Hylan B gel): a new injectable remedy for treatment of vocal fold insufficiency--an animal study. Acta Otolaryngol (1999) 0.95
Polymorphisms in DNA repair genes as risk factors for spina bifida and orofacial clefts. Am J Med Genet A (2005) 0.95
Automatic ankle pressure measurements using PPG in ankle-brachial pressure index determination. Eur J Vasc Endovasc Surg (2005) 0.95
Astrocytomas and choroid plexus tumors in two families with identical p53 germline mutations. J Neuropathol Exp Neurol (1998) 0.94
[Coagulation factor VII deficiency in 3 patients with trisomy 8]. Ann Genet (1974) 0.94
The use of surface spreading in the pachytene analysis of a human t (Y;17) reciprocal translocation. Cytogenet Cell Genet (1982) 0.94
Local recurrence of low rectal cancer after abdominoperineal and anterior resection. Br J Surg (1997) 0.93
[The r(14) syndrome. 3 new observations]. Ann Genet (1984) 0.93
[Translocation t(2q-; 21q+) in three generations]. Ann Genet (1968) 0.93
Proteoglycans and hyaluronan in human fetal membranes. Am J Obstet Gynecol (2001) 0.93
[Fetus in fetu and acardiac monster: can the similar patterns of these 2 malformations be explained by a common morphogenic mechanism?]. Arch Anat Cytol Pathol (1991) 0.93
Budesonide nasal spray as prophylactic treatment after polypectomy (a double blind clinical trial). J Laryngol Otol (1988) 0.93
Dramatic change in public attitudes towards vaccination during the 2009 influenza A(H1N1) pandemic in France. Euro Surveill (2013) 0.92
Short- and long-term impact of body mass index on laparoscopic rectal cancer surgery. Colorectal Dis (2013) 0.92
[T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter]. Ann Genet (1973) 0.92
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12. Nat Genet (1994) 0.92
Involvement of the Syk-mTOR pathway in follicular lymphoma cell invasion and angiogenesis. Leukemia (2011) 0.92
[Partial deletion of the long arm of a group D (13-15) chromosome :Dq-]. Ann Genet (1967) 0.92
The catabolic fate of hyaluronic acid. Connect Tissue Res (1986) 0.91
Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1 alpha deficiency. Hum Genet (1997) 0.91
Prevalence of treated diabetes: Geographical variations at the small-area level and their association with area-level characteristics. A multilevel analysis in Southeastern France. Diabetes Metab (2010) 0.91
The congenital anomalies registry in Belarus: a tool for assessing the public health impact of the Chernobyl accident. Reprod Toxicol (2003) 0.89
Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie Infantile. J Neurol Sci (1986) 0.89
Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome. Neuropediatrics (1993) 0.89
[Partial monosomy of a C group chromosome (Cp-)]. Ann Genet (1968) 0.89
Cytogenetic monitoring of a village population potentially exposed to a low level of environmental pollutants. Phase 1:SCE analysis. Mutat Res (1993) 0.88
Labour induces increased concentrations of biglycan and hyaluronan in human fetal membranes. Placenta (2006) 0.88
[Laparoscopic pancreatectomy: report of 22 cases]. Ann Chir (2003) 0.88
Dietary intakes and vitamin status of a sample of homeless people in Paris. Eur J Clin Nutr (2002) 0.88
The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52. Genomics (1992) 0.88
Abnormal phenotype in a child with a "balanced" translocation 8/12 in mosaic state. Am J Med Genet (1987) 0.88
Occurrence of total aflatoxins, ochratoxin A and deoxynivalenol in foodstuffs available on the Lebanese market and their impact on dietary exposure of children and teenagers in Beirut. Food Addit Contam Part A Chem Anal Control Expo Risk Assess (2009) 0.88
Thanatophoric dysplasia of identical twins. Am J Med Genet (1984) 0.88
Morbidity and functional outcome after double dynamic graciloplasty for anorectal reconstruction. Br J Surg (2000) 0.88
Learned caloric adjustment of human intake. Appetite (1989) 0.87
[Efficiency of psychological debriefing in preventing post-traumatic stress disorders]. Rev Epidemiol Sante Publique (2004) 0.87
Comparison of the karyotypes of four Cercopithecoidae: Papio papio, P. anubis, Macaca mulatta, and M. fascicularis. Cytogenet Cell Genet (1979) 0.87
European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. Am J Med Genet (1998) 0.87
The diagnosis of mucopolysaccharidoses by electron microscopy of skin biopsies. J Cutan Pathol (1975) 0.87
X-linked myopathy with excessive autophagy: a clinicopathological study of five new families. Neuromuscul Disord (2001) 0.87
Viral infections and chemical exposures as risk factors for hepatocellular carcinoma in Vietnam. Int J Cancer (1993) 0.87
Malignant melanoma of the hepatic and common bile ducts. A case report and review of the literature. Arch Pathol Lab Med (1991) 0.87