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Neoplasia endocrina múltiple tipo 2B
(Instituto de Cirugía de la Facultad de Medicina de la Universidad Austral de Chile y el Servicio de Cirugía del Hospital Clínico Regional de Valdivia, 2018)
Reply to Hunter's letter on the "Misuse of the Descriptor "Marfanoid""
(Wiley-liss, 2008-07-01)
Reply to Hunter's letter on the "Misuse of the Descriptor "Marfanoid""
(Wiley-liss, 2008-07-01)
Metacarpophalangeal pattern profile in Marfan syndrome and Marfan-like patients
(1997-10-17)
Marfan syndrome (MFS) is an autosomal dominant trait due to mutations in the fibrillin gene (FBN1). The MFS expressivity is variable, and its diagnosis relies completely on clinical criteria. Atypical cases and Marfan- ...
Metacarpophalangeal pattern profile in Marfan syndrome and Marfan-like patients
(Wiley-lissHobokenEUA, 1997)
Marfanoid features and X-linked mental retardation associated with craniofacial abnormalities: the Lujan-Fryns syndrome
(Academia Brasileira de Neurologia - ABNEURO, 2013-01-01)
Reply to Hunter's letter on the "Misuse of the Descriptor "Marfanoid""
(Wiley-liss, 2014)
A newly recognized syndrome of marfanoid habitus; Long face; Hypotelorism; Long, thin nose; Long, thin hands and feet; and a specific pattern of language and learning disabilities
(Wiley-Blackwell, 2007-12-15)
Here, we report on a newly recognized syndrome in a Brazilian family with three affected women, who had a Marfanoid habitus; long face; hypotelorism; long, thin nose; long, thin hands and feet; and language and learning ...
A newly recognized syndrome of marfanoid habitus; Long face; Hypotelorism; Long, thin nose; Long, thin hands and feet; and a specific pattern of language and learning disabilities
(Wiley-Blackwell, 2007-12-15)
Here, we report on a newly recognized syndrome in a Brazilian family with three affected women, who had a Marfanoid habitus; long face; hypotelorism; long, thin nose; long, thin hands and feet; and language and learning ...