L Vinken

Author PubWeight™ 8.79^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	The Coffin syndrome.	Hum Genet	1977	1.38
2	The Aarskog syndrome.	Hum Genet	1978	1.01
3	The Coffin-Lowry syndrome. A study of two new index patients and their families.	Eur J Pediatr	1984	0.90
4	Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype.	Hum Genet	1979	0.83
5	Triploid-diploid mosaïcism in a deeply mentally retarded adult.	Ann Genet	1980	0.82
6	Mosaic tetrasomy 21 in severe mental handicap.	Eur J Pediatr	1982	0.81
7	Dysosteosclerosis in a mentally retarded boy.	Acta Paediatr Belg	1980	0.77
8	Thrombocytopenia in the Brachmann-de Lange syndrome.	Am J Med Genet	1994	0.77
9	Effect of balanced X/autosome translocations on sexual and physical development. A personal experience in 4 patients.	Clin Genet	1985	0.77
10	Profound mental retardation, characteristic facies with midfacial hypoplasia and premature frontotemporal balding, muscular hypotrophy, and small patellae in two unrelated male patients.	J Med Genet	1993	0.75
11	Ocular symptoms in Cornelia de Lange syndrome.	Bull Soc Belge Ophtalmol	1977	0.75
12	Acrocentric/18p translocation in two mentally retarded males. Delineation of the adult phenotype.	Ann Genet	1986	0.75
13	Ectomorphic habitus, severe mental retardation and characteristic face: a new MCA/MR syndrome?	Am J Med Genet	1994	0.75
14	The otopalatodigital syndrome.	Acta Paediatr Belg	1978	0.75
15	Characterization of amino acids Arg, Ser and Thr at position 70 within HIV-1 reverse transcriptase.	Acta Clin Belg	2014	0.75