Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?William Reardon; I. Karen Temple; Barry Jones; Michael Baraitser · 1990

Craniofrontonasal dysplasiaL. Kapusta; H. G. Brunner; B. C. J. Hamel · 1992

Craniofrontonasal dysplasiaD.J.A. Orr; S. Slaney; G.J. Ashworth; M.D. Poole · 1997

Craniofrontonasal dysplasia: Genetic heterogeneity?M. L. Kwee; D. Lindhout · 1984

Craniofrontonasal dysplasia.Young, I D · Journal of Medical Genetics · 1987

Craniofrontonasal DysplasiaWolfswinkel, Erik Matthew; Weathers, William M.; Correa, Bryan; Buchanan, Edward P.; Hollier, Larry H. · Journal of Craniofacial Surgery · 2013

Craniofrontonasal dysplasia: clinical and genetic analysisChristina M. Sax; David B. Flannery · 1986

The Holt-Oram syndrome.Hurst, J A; Hall, C M; Baraitser, M · Journal of Medical Genetics · 1991

Johanson-Blizzard syndrome.Hurst, J A; Baraitser, M · Journal of Medical Genetics · 1989

Three patients with the osteochondrodysplasia and hypertrichosis syndrome - Cantu syndromeRosser, E M; Kaariainen, H; Hurst, J A; Baraitser, M; Hall, C M; Clayton, P; Leonard, J V · Clinical Dysmorphology · 1998

Balanced t(6;8)(6p8p;6q8q) and the CHARGE association.Hurst, J A; Meinecke, P; Baraitser, M · Journal of Medical Genetics · 1991

A familial syndrome of microcephaly, sparse hair, mental retardation, and seizures.van Haeringen, A; Hurst, J A; Savidge, R; Baraitser, M · Journal of Medical Genetics · 1990

Two brothers with heart defects and limb shortening: case reports and review.Reardon, W; Hurst, J; Farag, T I; Hall, C; Baraitser, M · Journal of Medical Genetics · 1990

De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies.Temple, I K; Hurst, J A; Hing, S; Butler, L; Baraitser, M · Journal of Medical Genetics · 1990

Barth syndromeJefferies, John L. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2013

Congenital microcephalyAlcantara, Diana; O'Driscoll, Mark · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014

Introduction: Brain malformationsMirzaa, Ghayda M.; Paciorkowski, Alex R. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014

Pontocerebellar hypoplasiaRudnik-Schöneborn, Sabine; Barth, Peter G.; Zerres, Klaus · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014

Pallister-Killian syndromeIzumi, Kosuke; Krantz, Ian D. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014

Cytogenetic highlights and transitionsSpinner, Nancy B. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016

IntroductionAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016

Publication schedule for 2016American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016