Search Results - "Hood, O J"

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  1. 1

    Abnormal ossification in thanatophoric dysplasia by Horton, W A, Hood, O J, Machado, M A, Ahmed, S, Griffey, E S

    Published in Bone (New York, N.Y.) (1988)
    “…Thanatophoric dysplasia (TD) is a lethal human bone dysplasia characterized by severe dwarfism. It pathogenesis is thought to involve an abnormal ossifying…”
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  2. 2

    Proximal duplications of chromosome 15: clinical dilemmas by Hood, O J, Rouse, B M, Lockhart, L H, Bodensteiner, J B

    Published in Clinical genetics (01-03-1986)
    “…The apparently rare cytogenetic abnormality of partial trisomy 15 was diagnosed by the authors in a patient presenting with developmental retardation,…”
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    Tics and tremors by Golden, G S, Hood, O J

    Published in The Pediatric clinics of North America (01-02-1982)
    “…Tics are the most common movement disorder of childhood. The single tic, or habit spasm, is benign and self-limited. Complex tic disorders include other…”
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  5. 5

    Growth hormone therapy in achondroplasia by Horton, W A, Hecht, J T, Hood, O J, Marshall, R N, Moore, W V, Hollowell, J G

    Published in American journal of medical genetics (01-03-1992)
    “…A pilot study was carried out to examine the safety and efficacy of recombinant human growth hormone for growth-promoting therapy of achondroplasia. The data…”
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  6. 6

    Obesity in achondroplasia by Hecht, J T, Hood, O J, Schwartz, R J, Hennessey, J C, Bernhardt, B A, Horton, W A

    Published in American journal of medical genetics (01-11-1988)
    “…Obesity is a significant and potentially serious health problem in achondroplasia. Body mass indices, weight-to-square of the height ratio (W/H2), and triceps…”
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  7. 7

    Unbalanced translocation (15;17)(q13;13.3) with apparent Prader-Willi syndrome but without Miller-Dieker syndrome by Elder, F F, Nichols, M M, Hood, O J, Harrison, 3rd, W R

    Published in American journal of medical genetics (01-03-1985)
    “…We studied after death a 3-month-old girl whose karyotype was 45,XX,-15,-17,+der(17),t(15;17)(q13;p13.3) and thus combines abnormalities of chromosome 15…”
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  8. 8

    Multiple congenital anomalies associated with a 47,XXX chromosome constitution by Hood, O J, Hartwell, E A, Shattuck, K E, Rosenberg, H S

    Published in American journal of medical genetics (01-05-1990)
    “…An infant with a 47,XXX chromosome constitution, who died shortly after birth, had laryngeal atresia, pulmonary hypoplasia, craniofacial anomalies, urogenital…”
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