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Clinical Dysmorphology|September 15, 2004
Congenital cardiac disease as a core feature of cranio-osteoarthropathySusan O'Connell, Mohnish Suri, Desmond Duff, et al.Clinical Dysmorphology|September 15, 2004
Filippi syndrome: two cases with ectodermal features, expanding the phenotypeS Sharif, D DonnaiClinical Dysmorphology|September 15, 2004
Catel-Manzke syndrome: a case report of a female with severely malformed hands and feet. An extension of the phenotype or a new syndrome?J H W Clarkson, T Homfray, C W Heron, et al.Clinical Dysmorphology|July 1, 1994
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome without and with associated features: two separate entities?E H Strübbe, C W Cremers, W N Willemsen, et al.Clinical Dysmorphology|July 1, 1994
A distinct autosomal dominant craniosynostosis-brachydactyly syndromeI A Glass, S Chapman, A D HockleyClinical Dysmorphology|July 1, 1994
Anterior segment anomalies of the eye, clefting and skeletal abnormalities in two sibs of consanguineous parents: Michels syndrome or new syndrome?L I al Gazali, J al Talabani, A Mosawi, et al.Clinical Dysmorphology|January 1, 1994
Greig cephalopolysyndactyly syndrome in a large family: a comparison of the clinical signs with those described in the literatureM G Ausems, P F Ippel, P A Renardel de LavaletteClinical Dysmorphology|August 31, 2019
A novel missense variant in the BBS7 gene underlying Bardet-Biedl syndrome in a consanguineous Pakistani familyAmir Hayat, Atif Ahmad Khan, Abdur Rauf, et al.Clinical Dysmorphology|June 11, 2008
Bilateral camptodactyly and recurrent patellar dislocation: a new sign of 22q11 deletions or an independent dominant disorder?Mary C O'Driscoll, Jill Clayton-SmithClinical Dysmorphology|August 25, 2022
Neurodevelopmental disorder with microcephaly, ataxia, and seizures syndrome: expansion of the clinical spectrumKadri Karaer, Derya Karaer, Zafer Yüksel, et al.Pageof 117