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Clinical Dysmorphology|October 25, 2000
Multiple subcutaneous granular-cell tumours in a patient with Noonan syndromeD R Lohmann, G Gillessen-KaesbachClinical Dysmorphology|January 11, 2001
An Asian girl with a 'milder' form of the Hydrolethalus syndromeV Shotelersuk, V Punyavoravud, S Phudhichareonrat, et al.Clinical Dysmorphology|January 11, 2001
An unusual fetus with complete absence of thoracic, lumbar and sacral vertebrae, bilateral renal agenesis, VSD, meningomyelocele, imperforate anus, and teratomaC N Semerci, I Bebitoglu, A Kaçar, et al.Clinical Dysmorphology|January 11, 2001
A case of Acro-renal-mandibular syndrome in an 18 week male fetusE S Tobias, Patrick WJA, J R MacKenzie, et al.Clinical Dysmorphology|January 11, 2001
Severe terminal transverse limb reduction defects in homozygous Southeast-Asian alpha-thalassaemia-1C P ChenClinical Dysmorphology|October 23, 2001
Absent lacrimal ducts, distichiasis, dysmorphic features, and brachydactyly: a case reportM Holder-Espinasse, M C de Blois, L Faivre, et al.Clinical Dysmorphology|October 23, 2001
Clinical phenotypes of nine cases of Kabuki syndrome from New ZealandJ McGaughran, S Aftimos, C Jefferies, et al.Clinical Dysmorphology|October 23, 2001
Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factorT J de Ravel, E Legius, H Brems, et al.Clinical Dysmorphology|October 23, 2001
Non-progressive mental retardation and peripheral neuropathy in a mother and her sonC Longman, J Tolmie, R McWilliamClinical Dysmorphology|August 24, 2000
Char syndrome: a new family and review of the literature emphasising the presence of symphalangism and the variable phenotypeE Sweeney, A Fryer, M WaltersPageof 117