Zobrazeno 1 - 10
of 12
pro vyhledávání: '"H. H. Stroud"'
Publikováno v:
Clinical Genetics. 17:428-432
A de novo partial 13q monosomy is reported in a severely affected 8-year-old female with the karyotype 46,XX,del(13)(q32). Abnormal features included mental retardation, delayed development, microcephaly, encephalocele, hearing loss, hypertelorism, p
Publikováno v:
Pediatrics. 13:140-145
A case of convulsions in an infant requiring pyridoxine for their control has been described. On oral dosage of pyridoxine 2 mg./day, seizures have now been controlled for 21 months, with no increase in dosage being required. A continuing need for py
Autor:
H H, Stroud
Publikováno v:
Delaware medical journal. 59(3)
Publikováno v:
Clinical genetics. 17(6)
A de novo partial 13q monosomy is reported in a severely affected 8-year-old female with the karyotype 46,XX,del(13)(q32). Abnormal features included mental retardation, delayed development, microcephaly, encephalocele, hearing loss, hypertelorism, p
Autor:
H H, Stroud
Publikováno v:
Delaware medical journal. 42(9)
Autor:
H H, Stroud
Publikováno v:
Delaware medical journal. 41(11)
Publikováno v:
Pediatrics. 13(2)
Autor:
H H, Stroud
Publikováno v:
Delaware medical journal. 42(2)
Publikováno v:
Journal of Computer Assisted Tomography. 3:291
Autor:
H. H. Stroud, R. E. Bowman
Publikováno v:
Journal of the Chemical Society (Resumed). :1342