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Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B

Nature genetics, 2004-11, Vol.36 (11), p.1159-1161

2004

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Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

Human molecular genetics, 1995-04, Vol.4 (4), p.583-587

1995

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

The American journal of psychiatry, 1997-05, Vol.154 (5), p.691-693

1997

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Malformations in children with cancer

American journal of medical genetics. Part A, 2006-04, Vol.140A (8), p.932-932

Méhes, Károly

2006

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Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency

Journal of inherited metabolic disease, 2009-12, Vol.32 (Suppl 1), p.15-19

2009

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Increased prevalence of factor V Leiden mutation in neonatal intracranial haemorrhage

European journal of pediatrics, 1998-03, Vol.157 (3), p.261-261

1998

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Facial measurements in the newborn

Journal of medical genetics, 1991-01, Vol.28 (1), p.65-65

Mehes, K

1991

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Umbilical venous catheterization and development of Banti syndrome: the possible role of the factor V Leiden mutation

European journal of pediatrics, 1998-08, Vol.157 (8), p.696-696

1998

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Association of supernumerary nipples with other anomalies

The Journal of pediatrics, 1979-08, Vol.95 (2), p.274-275

Méhes, K

1979

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

Journal of medical genetics, 1993-01, Vol.30 (1), p.76-77

MEHES, K

1993

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Physicians' Attitudes Regarding Down Syndrome

Journal of child neurology, 1996-01, Vol.11 (1), p.66-69

1996

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Association of supernumerary nipples with renal anomalies

The Journal of pediatrics, 1987-09, Vol.111 (3), p.412-413

1987

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Association of supernumerary nipples with other anomalies

The Journal of pediatrics, 1983, Vol.102 (1), p.161-161

Mèhes, K.

1983

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Inherited ring chromosomes : an analysis of published cases

Human genetics, 1991-07, Vol.87 (3), p.320-324

1991

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No latent chromosome damage in oxygen-exposed premature neonates

Journal of human genetics, 1999-01, Vol.44 (1), p.40-42

1999

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

American journal of medical genetics, 2004-12, Vol.131A (2), p.121-126

2004

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Epithelial Ca2+ channel (ECAC1) in autosomal dominant idiopathic hypercalciuria

Nephrology, dialysis, transplantation, 2002-09, Vol.17 (9), p.1614-1620

2002

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Urántartalmú köszenek genetikai típusai

Földtani Közlöny, 1984, Vol.114 (2), p.215-223

MEHES, K

1984

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

American journal of medical genetics, 1996-10, Vol.65 (1), p.82-88

1996

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Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia

European journal of pediatrics, 2002-11, Vol.161 (11), p.619-622

2002

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A possible mosaic form of delayed centromere separation and aneuploidy

Human genetics, 1992-02, Vol.88 (4), p.477-478

1992

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

American journal of medical genetics. Part A, 2005-06, Vol.135A (3), p.320-323

2005

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

Clinical genetics, 2000-09, Vol.58 (3), p.177-180

2000

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

European journal of human genetics : EJHG, 2003-05, Vol.11 (5), p.375-379

2003

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Head measurements in newborn infants

Journal of craniofacial genetics and developmental biology, 1987, Vol.7 (3), p.295

Méhes, K

1987

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Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

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

Malformations in children with cancer

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency

Increased prevalence of factor V Leiden mutation in neonatal intracranial haemorrhage

Facial measurements in the newborn

Umbilical venous catheterization and development of Banti syndrome: the possible role of the factor V Leiden mutation

Association of supernumerary nipples with other anomalies

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

Physicians' Attitudes Regarding Down Syndrome

Association of supernumerary nipples with renal anomalies

Association of supernumerary nipples with other anomalies

Inherited ring chromosomes : an analysis of published cases

No latent chromosome damage in oxygen-exposed premature neonates

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

Epithelial Ca2+ channel (ECAC1) in autosomal dominant idiopathic hypercalciuria

Urántartalmú köszenek genetikai típusai

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

Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia

A possible mosaic form of delayed centromere separation and aneuploidy

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

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

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

Head measurements in newborn infants

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