Károly Méhes (1936–2007)
Progressive and symmetric supraorbital hyperostosis with bony and soft tissue overgrowth in an Ethiopian female: A newly recognized overgrowth syndrome?
The clinical atlas of Greig cephalopolysyndactyly syndrome
Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia
Pituitary abnormalities in Prader–Willi syndrome and early onset morbid obesity
A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11
Cranial nerve manifestations in CHARGE syndrome
X-linked congenital ataxia: A new locus maps to Xq25-q27.1
3q29 interstitial microduplication: A new syndrome in a three-generation family
Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: Under-representation of the common c.985 A>G mutation in the New York state population
Genotype–phenotype analysis and natural history of left ventricular hypertrophy in LEOPARD syndrome
A quantitative assessment of tremor and ataxia in FMR1 premutation carriers using CATSYS
Duplication of 17(p11.2p11.2) in a male child with autism and severe language delay
Autosomal dominant gigantiform cementoma associated with bone fractures
Two new Brazilian patients with Gómez–López-Hernández syndrome: Reviewing the expanded phenotype with molecular insights
Second case of Beare–Stevenson syndrome with an FGFR2 Ser372Cys mutation
Perrault syndrome: Report of four new cases, review and exclusion of candidate genes
Follicle stimulating and leutinizing hormones, estradiol and testosterone in Prader–Willi syndrome
Segmental hemangioma: An important clinical term
Segmental hemangioma: The misuse of a term
Oculocerebrocutaneous syndrome: An update