D. Lacombe

Neurodevelopmental outcome following prenatal diagnosis of an isolated anomaly of the corpus callosum

M. Duyme, C. Capron, N. Fries, 2011, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Clinical and molecular genetic spectrum of autosomal dominant Emery‐Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

E. Mercuri, K. Bushby, F. Muntoni, 2000, Annals of neurology.

Leber’s optic neuropathy associated with disseminated white matter disease: A case report and review

B. Brochet, M. Martin-Négrier, C. Goizet, 2009, Clinical Neurology and Neurosurgery.

Successful laparoscopic operation of bilateral pheochromocytoma in a patient with Beckwith-Wiedemann syndrome

P. Gosse, P. Tauzin-Fin, P. Barat, 2002, Journal of Human Hypertension.

Prenatal Diagnosis of Hypochondroplasia: Three-Dimensional Multislice Computed Tomography Findings and Molecular Analysis

F. Diard, O. Bonnefoy, D. Gaye, 2005, Fetal Diagnosis and Therapy.

Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling

D. Lacombe, C. Yardin, S. Briault, 2002, Prenatal diagnosis.

Prenatal diagnosis of cerebral and extracerebral high‐flow lesions revealing familial capillary malformation‐arteriovenous malformation (CM‐AVM) syndrome

L. Guibaud, A. Lacalm, A. Fichez, 2018, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Bilateral Macular Detachment Caused by Bilateral Optic Nerve Malformation in a Papillorenal Syndrome Due to a New Pax2 Mutation

C. Antignac, J. Korobelnik, C. Combe, 2008, European journal of ophthalmology.

[Neurological, dermatological and biological manifestations of porphyria variegata. A study of 3 families of Italian origin in Marseilles area].

J. Lamoril, D. Lacombe, G. Topi, 1992, Revue neurologique (Paris).

Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutation.

J. Korobelnik, C. Combe, D. Lacombe, 2008, European journal of ophthalmology.