Nancy Mizue Kokitsu-Nakata

Author PubWeight™ 5.47^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Further delineation of Kabuki syndrome in 48 well-defined new individuals.	Am J Med Genet A	2005	1.17
2	Oculoauriculovertebral spectrum: report of nine familial cases with evidence of autosomal dominant inheritance and review of the literature.	Clin Dysmorphol	2009	1.05
3	Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears.	Am J Hum Genet	2013	1.02
4	Auriculo-condylar syndrome: additional patients.	Am J Med Genet	2002	0.86
5	Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndrome.	Am J Med Genet A	2014	0.77
6	Saethre-Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7.	Am J Med Genet A	2012	0.75
7	Aural atresia and microtia in Kabuki syndrome.	Am J Med Genet A	2003	0.75
8	Speech-language and hearing findings in the cardio-facial-cutaneous syndrome.	Pro Fono	2004	0.75
9	Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case.	Am J Med Genet A	2003	0.75