Published in Clin Genet on November 01, 1982
Imaging the craniocervical junction. Childs Nerv Syst (2008) 1.38
Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice. Dev Dyn (2008) 0.90
Coexistence of left internal carotid agenesis, klippel-feil syndrome and postaxial polydactyly. Pol J Radiol (2015) 0.75
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Pervasive density-dependent recruitment enhances seedling diversity in a tropical forest. Nature (2000) 5.62
Current databases on biological variation: pros, cons and progress. Scand J Clin Lab Invest (1999) 4.30
Neuronal correlates of parametric working memory in the prefrontal cortex. Nature (1999) 3.98
Somatosensory discrimination based on cortical microstimulation. Nature (1998) 2.85
Sensing without touching: psychophysical performance based on cortical microstimulation. Neuron (2000) 1.86
The voltage sensitive Lc-type Ca2+ channel is functionally coupled to the exocytotic machinery. Proc Natl Acad Sci U S A (1999) 1.78
Evaluation of a new serodiagnostic tuberculosis test based on immunoglobulin A detection against Kp-90 antigen. Int J Tuberc Lung Dis (2000) 1.64
Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia. J Invest Dermatol (1999) 1.58
EEG interhemispheric correlation after callosotomy: one case study. Percept Mot Skills (1995) 1.57
Inherited congenital normofunctional testicular hyperplasia and mental deficiency. A corroborative study. Hum Genet (1978) 1.56
Evaluation of a rapid immunochromatographic assay for the detection of Legionella antigen in urine samples. Eur J Clin Microbiol Infect Dis (1999) 1.50
[Latin-American consensus document on irritable bowel syndrome]. Gastroenterol Hepatol (2004) 1.42
The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation. Hum Genet (1984) 1.40
Molecular characterization of the fragile-X syndrome in the Mexican population. Arch Med Res (1995) 1.40
A set of recombinant antigens from Echinococcus granulosus with potential for use in the immunodiagnosis of human cystic hydatid disease. Clin Exp Immunol (2003) 1.33
Risk factors for nosocomial pneumonia in critically ill trauma patients. Crit Care Med (2001) 1.30
Familial inv(1) (p3500q21.3) associated with azoospermia. Hum Genet (1984) 1.28
Inherited congenital normofunctional testicular hyperplasia and mental deficiency. Hum Genet (1976) 1.27
Crouzon with acanthosis nigricans. Further delineation of the syndrome. Clin Genet (2007) 1.27
Peutz-Jeghers syndrome with feminizing sertoli cell tumor. Cancer (1980) 1.21
Evaluation of a fluorescence hybridisation assay using peptide nucleic acid probes for identification and differentiation of tuberculous and non-tuberculous mycobacteria in liquid cultures. Eur J Clin Microbiol Infect Dis (2000) 1.17
Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomalies. Clin Genet (1982) 1.15
A distinct osteochondrodysplasia with hypertrichosis- Individualization of a probable autosomal recessive entity. Hum Genet (1982) 1.14
Water-borne transmission of chloramphenicol-resistant Salmonella typhi in Mexico. Lancet (1973) 1.14
The reference change value: a proposal to interpret laboratory reports in serial testing based on biological variation. Scand J Clin Lab Invest (2004) 1.12
Evaluation of allergic and serological tests for diagnosing Brucella melitensis infection in sheep. J Clin Microbiol (1994) 1.09
Bone disease in predialysis, hemodialysis, and CAPD patients: evidence of a better bone response to PTH. Kidney Int (1995) 1.09
3-M slender-boned nanism. An intrauterine growth retardation syndrome. Am J Dis Child (1981) 1.08
Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder. Clin Genet (1980) 1.07
Cardiovascular autonomic dysfunction in sickle cell anemia: a possible risk factor for sudden death? Clin Auton Res (1997) 1.07
Tetrasomy 18p: a distinctive syndrome. Ann Genet (1984) 1.05
RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease. J Med Genet (2000) 1.05
Comparison of a nonradiometric system with Bactec 12B and culture on egg-based media for recovery of mycobacteria from clinical specimens. Eur J Clin Microbiol Infect Dis (1998) 1.03
Intrathymic signals in thymocytes are mediated by p38 mitogen-activated protein kinase. J Immunol (1996) 1.02
Categorical perception of somesthetic stimuli: psychophysical measurements correlated with neuronal events in primate medial premotor cortex. Cereb Cortex (1997) 1.00
Potential impact of American Diabetes Association (2000) criteria for diagnosis of gestational diabetes mellitus in Spain. Diabetologia (2005) 1.00
Gerodermia osteodysplastica hereditaria: report of three affected brothers and literature review. Am J Med Genet (1979) 1.00
Functional properties of primate putamen neurons during the categorization of tactile stimuli. J Neurophysiol (1997) 0.97
De novo t(4;5)(q3100;q2200) with del(5)(q1500q2200). Tentative delineation of a 5q monosomy syndrome and assignment of the critical segment. Clin Genet (1985) 0.97
Evaluation of Meridian ImmunoCard Mycoplasma test for the detection of Mycoplasma pneumoniae-specific IgM in paediatric patients. Scand J Infect Dis (1998) 0.95
A new form of hypertrichosis inherited as an X-linked dominant trait. Hum Genet (1984) 0.94
[Becker nevus syndrome]. Actas Dermosifiliogr (2007) 0.94
Comparative evaluation of two commercial assays for direct detection of Mycobacterium tuberculosis in respiratory specimens. Eur J Clin Microbiol Infect Dis (1998) 0.94
Efficacy of preoperative diagnostic imaging localization of technetium 99m-sestamibi scintigraphy in hyperparathyroidism. Surgery (1997) 0.91
Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1. Nat Genet (1995) 0.91
Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRs. Hum Biol (2000) 0.91
(CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French-German population. Eur J Hum Genet (1999) 0.90
Evidence for autosomal recessive inheritance of costovertebral dysplasia. Clin Genet (1971) 0.90
Platelet ultrastructural morphometry for diagnosis of partial delta-storage pool disease in patients with mild platelet dysfunction and/or thrombocytopenia of unknown origin. A study of 24 cases. Haematologica (2000) 0.89
In vitro infection of murine macrophage by Leishmania brasiliensis. Mechanism of penetration. Int Arch Allergy Appl Immunol (1977) 0.89
MHC class II sequences of susceptibility and protection in Mexicans with autoimmune hepatitis. J Hepatol (1998) 0.89
[Localization by bone SPET of osteoid osteoma in the vertebral lamina]. Rev Esp Med Nucl (1999) 0.89
On a prezygotic origin of normal/balanced translocation mosaics. Ann Genet (1986) 0.89
Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome. Am J Med Genet (1997) 0.89
Terrible triad of the elbow--role of the coronoid process: a case report. J Orthop Surg (Hong Kong) (2005) 0.88
A new psychomotor retardation syndrome with peculiar facies and marfanoid habitus. Clin Genet (1984) 0.88
Caspofungin: a new therapeutic option for fungal endocarditis. Clin Microbiol Infect (2005) 0.88
Midline facial defect as a teratogenic effect of metronidazole. Birth Defects Orig Artic Ser (1982) 0.88
Heterozygous expression in 3-M slender-boned nanism. Hum Genet (1979) 0.88
[Chromosome aberrations in 334 individuals with various types of abortion (including 144 couples)]. Rev Invest Clin (1985) 0.87
Autosomal recessive inheritance of atrichia congenita. Clin Genet (1980) 0.87
Maternal glucose tolerance status influences the risk of macrosomia in male but not in female fetuses. J Epidemiol Community Health (2008) 0.86
Analgesia produced by intrathecal administration of the kappa opioid agonist, U-50,488H, on formalin-evoked cutaneous pain in the rat. Eur J Pharmacol (1990) 0.86
Idiotypic modulation of the antibody response of mice to Echinococcus granulosus antigens. Immunology (1995) 0.86
[De novo del (2) (q2300q24.1)]. Bol Med Hosp Infant Mex (1986) 0.86
Familial simple ectopia lentis. A probable autosomal recessive form. Ophthalmic Paediatr Genet (1986) 0.85
Monosomy 20p due to a de novo del(20)(p12.2). Clinical and radiological delineation of the syndrome. Ann Genet (1985) 0.85
Approaches for providing target values to improve usefulness of external quality assessment scheme. The Spanish experience. Scand J Clin Lab Invest Suppl (1993) 0.85
Effect of exogenous fibrolytic enzyme on ruminal fermentation and digestibility of alfalfa and rye-grass hay fed to lambs. J Anim Sci (2002) 0.85
Association of RRM1 -37A>C polymorphism with clinical outcome in colorectal cancer patients treated with gemcitabine-based chemotherapy. Eur J Cancer (2011) 0.85
On atavisms and atavistic genes. Ann Genet (1985) 0.85
Oral-facial-digital syndrome with fibular aplasia: a new variant. Clin Genet (1993) 0.85
VEGF/PLGF induces leukemia cell migration via P38/ERK1/2 kinase pathway, resulting in Rho GTPases activation and caveolae formation. Leukemia (2007) 0.85
Cardiovascular autonomic neuropathy in type 1 diabetic patients with and without peripheral neuropathy. Diabetes Res Clin Pract (1998) 0.84
Categorization of somaesthetic stimuli: sensorimotor performance and neuronal activity in primary somatic sensory cortex of awake monkeys. Neuroreport (1996) 0.84
Reduction of Ca(2+) channel activity by hypoxia in human and porcine coronary myocytes. Cardiovasc Res (2002) 0.84
Constitutional del(5)(q23.3q31.1). Ann Genet (1987) 0.84
Predicting vertical dimension with cephalograms, for edentulous patients. Gerodontology (2005) 0.84
Silent microcephaly: a distinct autosomal dominant trait. Clin Genet (1983) 0.84
Increased adenosine deaminase activity in a patient with cartilage-hair hypoplasia. Ann Genet (1990) 0.83
Identification of upstream signals regulating interleukin-6 gene expression during in vitro treatment of human B cells with pokeweed mitogen. Blood (1994) 0.83
Inv(4)(p16q21). A five-generation pedigree with 24 carriers and no recombinants. Clin Genet (1987) 0.83
Autosomal dominant keratosis palmaris et plantaris with clinodactyly. Birth Defects Orig Artic Ser (1982) 0.83
Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:). Ann Genet (1979) 0.83