K. Méhes

发表

K. Méhes, 2004, Orvosi hetilap.

A nationwide evaluation of multiple congenital abnormalities in Hungary

J. Neel, K. Méhes, A. Czeizel, 1988, Genetic epidemiology.

Phenotypic manifestations of the OCTN2 V295X mutation: Sudden infant death and carnitine‐responsive cardiomyopathy in Roma families

B. Sumegi, K. Méhes, J. Bene, 2004, American journal of medical genetics. Part A.

Family investigations in idiopathic hypercalciuria

K. Méhes, F. Harangi, 2005, European Journal of Pediatrics.

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency

K. Méhes, B. Melegh, G. Mogyorósy, 2009, Journal of Inherited Metabolic Disease.

Agenesis of pancreas and gall-bladder in an infant of incest.

K. Méhes, K. Vámos, M. Goda, 1976, Acta paediatrica Academiae Scientiarum Hungaricae.

Maternal regulation of fetal growth.

K. Méhes, P. Tóth, K. Keszei, 1983, Acta paediatrica Hungarica.

Urinary hydroxyproline and glycosaminoglycan excretion in Down's syndrome

K. Méhes, L. Klujber, 2004, Zeitschrift für Kinderheilkunde.

Tel Hashomer camptodactyly syndrome: 12‐year follow‐up of a Hungarian patient and review

K. Méhes, B. Melegh, K. Hollódy, 2005, American journal of medical genetics. Part A.

Epithelial Ca(2+) channel (ECAC1) in autosomal dominant idiopathic hypercalciuria.

K. Méhes, R. Vennekens, B. Nilius, 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Cohen syndrome: a connective tissue disorder?

K. Méhes, M. Kardos, M. Horváth, 1988, American journal of medical genetics.

Bilateral coats retinopathy associated with aplastic anaemia and mild dyskeratotic signs.

K. Méhes, P. Kajtár, 1994, American journal of medical genetics.

Increased Frequency of the C3*F Allele and the Leiden Mutation of Coagulation Factor V in Patients with Severe Coronary Heart Disease Who Survived Myocardial Infarction

K. Méhes, L. Romics, B. Melegh, 2002, Experimental and Clinical Immunogenetics.

Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia

S. Mundlos, K. Méhes, E. Morava, 2002, European Journal of Pediatrics.

Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome

K. Méhes, E. Morava, M. Czakó, 2003, Clinical dysmorphology.

Excess of mild errors of morphogenesis in childhood lymphoblastic leukemia.

K. Méhes, D. Niethammer, P. Kajtár, 1998, American journal of medical genetics.

Physicians' Attitudes Regarding Down Syndrome

K. Méhes, R. Hermann, 1996, Journal of child neurology.

Preauricular pits in Hungary: epidemiologic and clinical observations.

K. Méhes, V. Meggyessy, 1982, Journal of craniofacial genetics and developmental biology.

Multiple mitochondrial DNA deletions and persistent hyperthermia in a patient with Brachmann-de Lange phenotype.

K. Méhes, B. Melegh, I. Gáti, 1996, American journal of medical genetics.

[Incidence and importance of minor abnormalities].

K. Méhes, E. Czeizel, F. Obál, 1975, Orvosi hetilap.

Intractable diarrhoea of infancy and latent otomastoiditis.

K. Méhes, M. Buša, 1981, Archives of disease in childhood.

Association of supernumerary nipples with other anomalies.

K. Méhes, B. Kaye, 1980, The Journal of pediatrics.

Down's syndrome with familial G-G translocation.

K. Méhes, 1969, Acta geneticae medicae et gemellologiae.

Premature centromere division: a possible manifestation of chromosome instability.

K. Méhes, E. Bühler, 1995, American journal of medical genetics.

Hypophosphatasia: screening and family investigations in an endogamous Hungarian village

K. Méhes, P. Kajtár, L. Klujber, 1972, Clinical genetics.

Down's syndrome: chromosome analysis of 362 cases in Hungary.

J. László, K. Méhes, E. Czeizel, 1977, Human heredity.

Dysmorphology in Children with Congenital Metabolic Disorders

K. Méhes, 1991, Acta paediatrica Japonica : Overseas edition.

Clinical manifestations of genetic instability overlap one another

K. Méhes, Károly Méhes, György Kosztolányi, 2008, Pathology & Oncology Research.

Mild errors of morphogenesis in malignancy: macroscopic manifestation of genetic instability?

K. Méhes, 2000, Medical and pediatric oncology.

Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B

N. Rahman, H. Firth, J. Tolmie, 2004, Nature Genetics.

Isolated hypospadias is not associated with signs of midline closure defects.

K. Méhes, 1998, American journal of medical genetics.

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.

K. Méhes, B. Hamel, B. Hamel, 1995, Human molecular genetics.

Cat-eye syndrome, a partial trisomy 22

K. Méhes, G. Stalder, H. Müller, 1972, Humangenetik.

Supernumerary digital flexion creases

K. Méhes, G. Kosztolányi, 2003, American Journal of Medical Genetics. Part A.

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation

K. Méhes, A. Schinzel, D. Kotzot, 2000, Clinical genetics.

Premature centromere division of a translocation-carrier autosome

K. Méhes, G. Kosztolányi, 1990, Human Genetics.

Parental centromere separation sequence and aneuploidy in the offspring

K. Méhes, K. Bajnóczky, 1988, Human Genetics.

Non-random centromere division: a mechanism of non-disjunction causing aneuploidy?

K. Méhes, 1978, Human heredity.

Delayed speech development, facial asymmetry, strabismus, and transverse ear lobe creases: a new syndrome?

K. Méhes, Hungary K Mehes, 1993, Journal of medical genetics.

[Sex chromosome aberration screening among male psychiatric patients (author's transl)].

K. Méhes, M. Trixler, G. Kosztolányl, 1976, Archiv fur Psychiatrie und Nervenkrankheiten.

Increased prevalence of factor V Leiden mutation in neonatal intracranial haemorrhage.

K. Méhes, B. Melegh, H. Losonczy, 1998, European journal of pediatrics.

Supernumerary nipples and urologic malignancies.

K. Méhes, F. Törzsök, V. Meggyessy, 1987, Cancer Genetics and Cytogenetics.

Minor malformations in the neonate.

K. Méhes, J. Mestyán, V. Knoch, 1983, Helvetica paediatrica acta.

Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation.

K. Méhes, G. Kosztolányi, J. Weisenbach, 1995, American journal of medical genetics.

Elements of morphology: Standard terminology for the nose and philtrum

R. Hennekam, R. Stevenson, K. Méhes, 2009, American journal of medical genetics. Part A.

Minor malformations in mental retardation of various aetiology.

K. Méhes, V. Meggyessy, M. Révhelyi, 1980, Acta paediatrica Academiae Scientiarum Hungaricae.

Informative morphogenetic variants in patients with schizophrenia and alcohol-dependent patients: beyond the Waldrop Scale.

K. Méhes, T. Tényi, M. Trixler, 1997, The American journal of psychiatry.

Informative Morphogenetic Variants in the Newborn Infant

K. Méhes, 1995 .

Association of supernumerary nipples with renal anomalies.

K. Méhes, V. Meggyessy, 1988, The Journal of pediatrics.

Association of Wilms tumour with spina bifida occulta

K. Méhes, P. Kajtár, J. Weisenbach, 1990, European Journal of Pediatrics.

Familial association of supernumerary nipple with renal cancer.

K. Méhes, 1996, Cancer genetics and cytogenetics.

Association of supernumerary nipples with other anomalies.

K. Méhes, 1979, The Journal of pediatrics.

Facial measurements in the newborn.

K. Méhes, 1991, Journal of medical genetics.

I-Cell Disease.

K. Méhes, E. Bühler, H. Hirt, 1970, The New England journal of medicine.

Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population.

K. Méhes, B. Melegh, E. Morava, 1999, American journal of medical genetics.

Minor morphological aberrations in children with isolated urinary tract malformations

K. Méhes, A. Pintér, 1990, European Journal of Pediatrics.

Plasma amino acid concentrations in healthy, full-term infants fed hydrolysate infant formula.

K. Méhes, V. Veitl, T. Decsi, 1996, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

Excess of Malignancies in Grandparents of Children With Malformations?

K. Méhes, K. Hadzsiev, G. Kosztolányi, 2006, Acta biologica Hungarica.

Inner canthal and intermamillary indices in the newborn infant.

K. Méhes, E. Kitzvéger, 1974, The Journal of pediatrics.

Palpebral fissure length in newborn infants.

K. Méhes, 1980, Acta paediatrica Academiae Scientiarum Hungaricae.

A simple score to facilitate detection of congenital disorders.

K. Méhes, 1977, Acta paediatrica Academiae Scientiarum Hungaricae.

Autosomal dominant inheritance of benign bilateral acromial dimples

K. Méhes, V. Meggyessy, 1987, Human Genetics.

Inherited ring chromosomes: an analysis of published cases

E. Hook, K. Méhes, G. Kosztolányi, 1991, Human Genetics.

Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion

K. Méhes, J. Bene, B. Melegh, 2003, European Journal of Human Genetics.

Incidence of major chromosomal abnormalities

K. Méhes, K. Bajnóczky, 1981, Clinical genetics.

[The significance of body measurements in the physical examination of infants and children].

K. Méhes, 1988, Orvosi hetilap.

Autosomal dominant inheritance of hypercalciuria

K. Méhes, Z. Szelid, 1980, European Journal of Pediatrics.

Familial benign copper deficiency.

K. Méhes, E. Petrovicz, 1982, Archives of disease in childhood.

Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias)

K. Méhes, G. Stalder, E. Bühler, 2004, Humangenetik.

Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy

K. Méhes, L. Seress, B. Melegh, 1999, Journal of Inherited Metabolic Disease.

Gastrointestinal Malformations, Associated Congenital Abnormalities, and Intrauterine Growth

K. Méhes, A. Tárnok, 2002, Journal of pediatric gastroenterology and nutrition.

Possible dominant inheritance of the idiopathic hypercalcemic syndrome.

K. Méhes, P. Tóth, Z. Szelid, 1975, Human heredity.

Changes in birth weight, birth length and head circumference of Hungarian children in the county Baranya between 1968 and 1979-1981.

K. Méhes, I. Járai, I. Dóber, 1993, Anthropologischer Anzeiger; Bericht uber die biologisch-anthropologische Literatur.

The predictive value of glucose utilization rate in neonatal hypoglycaemia of small-for-gestational-age infants.

K. Méhes, P. Tóth, I. Horváth, 1975, Acta paediatrica Academiae Scientiarum Hungaricae.

Non-random centromere division: analysis of G-banded human chromosomes.

K. Méhes, K. Bajnóczky, 1981, Acta biologica Academiae Scientiarum Hungaricae.

Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation.

Z. Szabo, K. Méhes, B. Melegh, 2008, Current medicinal chemistry.

Association of Wilms Tumor with Spinal Dysraphism

K. Méhes, P. Kajtár, J. Weisenbach, 2003, Pediatric hematology and oncology.

Increased prevalence of minor anomalies in childhood malignancy

K. Méhes, E. Signer, G. Stalder, 1985, European Journal of Pediatrics.

[Informative morphogenetic variants (minor congenital anomalies)].

K. Méhes, 1986, Orvosi Hetilap.

Minor malformations in the neonate: utility in screening infants at risk of hidden major defects.

K. Méhes, 1985, Progress in clinical and biological research.

Paternal trisomy 21 mosaicism and Down's anomaly

K. Méhes, 1973, Humangenetik.

Search for Factor V Arg306 Cambridge and Hong Kong Mutations in Mixed Hungarian Population Samples

K. Méhes, J. Bene, B. Melegh, 2003, Acta Haematologica.

Simian crease.

K. Méhes, 1972, Acta paediatrica Academiae Scientiarum Hungaricae.

Clinically recognisable autosomal anomalies in neonates.

K. Méhes, 1973, Lancet.

Chromatographic screening of 70,328 neonates for inborn errors of amino acid metabolism.

K. Méhes, E. Juhász, V. Ruszinkó, 1985, Acta paediatrica Hungarica.

Malformations in children with cancer

K. Méhes, 2006, American journal of medical genetics. Part A.

Clinically recognizable chromosomal abnormalities in newborn infants.

K. Méhes, K. Bajnóczky, 1990, American journal of medical genetics.