The Experts below are selected from a list of 495 Experts worldwide ranked by ideXlab platform
J P Keating - One of the best experts on this subject based on the ideXlab platform.
-
hyperphalangy and clinodactyly of the index Finger with pierre robin anomaly catel manzke syndrome a case report and review of the literature
Clinical Genetics, 2008Co-Authors: V Sundaram, Kutay Taysi, Alexis F Hartmann, Gary D Shackelford, J P KeatingAbstract:Mandibular hypoplasia, glossoptosis, U-shaped cleft palate (Pierre Robin anomaly), associated with bilateral index Finger Malformation and congenital heart disease are described in a male, newborn infant. Review of the features of seven previously published patients, in addition to the patient reported here, confirms the existence of a distinct dysmorphogenesis syndrome. Although all of these eight patients have been males, and most were sporadic, the etiology of this rare Malformation syndrome is unknown.
V Sundaram - One of the best experts on this subject based on the ideXlab platform.
-
hyperphalangy and clinodactyly of the index Finger with pierre robin anomaly catel manzke syndrome a case report and review of the literature
Clinical Genetics, 2008Co-Authors: V Sundaram, Kutay Taysi, Alexis F Hartmann, Gary D Shackelford, J P KeatingAbstract:Mandibular hypoplasia, glossoptosis, U-shaped cleft palate (Pierre Robin anomaly), associated with bilateral index Finger Malformation and congenital heart disease are described in a male, newborn infant. Review of the features of seven previously published patients, in addition to the patient reported here, confirms the existence of a distinct dysmorphogenesis syndrome. Although all of these eight patients have been males, and most were sporadic, the etiology of this rare Malformation syndrome is unknown.
Kutay Taysi - One of the best experts on this subject based on the ideXlab platform.
-
hyperphalangy and clinodactyly of the index Finger with pierre robin anomaly catel manzke syndrome a case report and review of the literature
Clinical Genetics, 2008Co-Authors: V Sundaram, Kutay Taysi, Alexis F Hartmann, Gary D Shackelford, J P KeatingAbstract:Mandibular hypoplasia, glossoptosis, U-shaped cleft palate (Pierre Robin anomaly), associated with bilateral index Finger Malformation and congenital heart disease are described in a male, newborn infant. Review of the features of seven previously published patients, in addition to the patient reported here, confirms the existence of a distinct dysmorphogenesis syndrome. Although all of these eight patients have been males, and most were sporadic, the etiology of this rare Malformation syndrome is unknown.
Alexis F Hartmann - One of the best experts on this subject based on the ideXlab platform.
-
hyperphalangy and clinodactyly of the index Finger with pierre robin anomaly catel manzke syndrome a case report and review of the literature
Clinical Genetics, 2008Co-Authors: V Sundaram, Kutay Taysi, Alexis F Hartmann, Gary D Shackelford, J P KeatingAbstract:Mandibular hypoplasia, glossoptosis, U-shaped cleft palate (Pierre Robin anomaly), associated with bilateral index Finger Malformation and congenital heart disease are described in a male, newborn infant. Review of the features of seven previously published patients, in addition to the patient reported here, confirms the existence of a distinct dysmorphogenesis syndrome. Although all of these eight patients have been males, and most were sporadic, the etiology of this rare Malformation syndrome is unknown.
Gary D Shackelford - One of the best experts on this subject based on the ideXlab platform.
-
hyperphalangy and clinodactyly of the index Finger with pierre robin anomaly catel manzke syndrome a case report and review of the literature
Clinical Genetics, 2008Co-Authors: V Sundaram, Kutay Taysi, Alexis F Hartmann, Gary D Shackelford, J P KeatingAbstract:Mandibular hypoplasia, glossoptosis, U-shaped cleft palate (Pierre Robin anomaly), associated with bilateral index Finger Malformation and congenital heart disease are described in a male, newborn infant. Review of the features of seven previously published patients, in addition to the patient reported here, confirms the existence of a distinct dysmorphogenesis syndrome. Although all of these eight patients have been males, and most were sporadic, the etiology of this rare Malformation syndrome is unknown.