Zobrazeno 1 - 3
of 3
pro vyhledávání: '"M J, Basehore"'
Autor:
Philippos C. Patsalis, S. Mcgee, Tao Wang, Maria Syrrou, Ephrat Levy-Lahad, Carolina Sismani, Angelos Alexandrou, Tom Walsh, M-C King, Charles E. Schwartz, L. Holloway, Fatima Abidi, M. J. Basehore, Lynne M. Bird, Gerald V. Raymond, Michael J. Friez, Rachel Michaelson-Cohen, Roger E. Stevenson, Cindy Skinner
Publikováno v:
Clinical Genetics. 87:461-466
Alpha-thalassemia intellectual disability, one of the recognizable X-linked disability syndromes, is characterized by short stature, microcephaly, distinctive facies, hypotonic appearance, cardiac and genital anomalies, and marked skewing of X-inacti
Autor:
M J, Basehore, R, Michaelson-Cohen, E, Levy-Lahad, C, Sismani, L M, Bird, M J, Friez, T, Walsh, F, Abidi, L, Holloway, C, Skinner, S, McGee, A, Alexandrou, M, Syrrou, P C, Patsalis, G, Raymond, T, Wang, C E, Schwartz, M-C, King, R E, Stevenson
Publikováno v:
Clinical genetics. 87(5)
Alpha-thalassemia intellectual disability, one of the recognizable X-linked disability syndromes, is characterized by short stature, microcephaly, distinctive facies, hypotonic appearance, cardiac and genital anomalies, and marked skewing of X-inacti
Autor:
V, Shashi, M S, Keshavan, T D, Howard, M N, Berry, M J, Basehore, E, Lewandowski, T R, Kwapil
Publikováno v:
Clinical genetics. 69(3)
Chromosome 22q11.2 deletion syndrome (22q11DS) is a common microdeletion syndrome associated with a markedly elevated risk of schizophrenia in adulthood. Cognitive impairments such as a low IQ and deficits in attention and executive function are comm