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    Principles of Genetic Testing

    Dr. Margaret A. Chen Ph.D., M.S. in Textbook of Clinical Pediatrics (2012)

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    Reference Work Entry At a glance

    Primary Hyperparathyroidism

    Dr. Haggi Mazeh M.D.… in Encyclopedia of Otolaryngology, Head and N… (2013)

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    Intraoperative Parathyroid Hormone (ioPTH) Monitoring

    Dr. Haggi Mazeh M.D.… in Encyclopedia of Otolaryngology, Head and N… (2013)

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    Reference Work Entry At a glance

    Preoperative Localization Studies

    Dr. Haggi Mazeh M.D.… in Encyclopedia of Otolaryngology, Head and N… (2013)

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    Reference Work Entry At a glance

    Minimally Invasive Parathyroidectomy

    Dr. Haggi Mazeh M.D.… in Encyclopedia of Otolaryngology, Head and N… (2013)

  6. No Access

    Reference Work Entry At a glance

    Multi-gland Disease

    Dr. Haggi Mazeh MD… in Encyclopedia of Otolaryngology, Head and N… (2013)

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    Bilateral Neck Exploration

    Dr. Haggi Mazeh M.D.… in Encyclopedia of Otolaryngology, Head and N… (2013)

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    Reference Work Entry In depth

    Intra-operative Parathyroid Hormone Monitoring Review

    Dr. Haggi Mazeh M.D., Dr. Alfred Simental… in Encyclopedia of Otolaryngology, Head and N… (2013)

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    Reference Work Entry In depth

    Radiologic Evaluation/Diagnostic Imaging of Paranasal Sinuses and Chronic Rhinosinusitis

    Dr. Girish Fatterpekar M.B.B.S.… in Encyclopedia of Otolaryngology, Head and N… (2013)

  10. No Access

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    Congenital Mixed Hearing Loss

    Dr. Brian S. Chen M.D.… in Encyclopedia of Otolaryngology, Head and N… (2013)

  11. No Access

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    Acquired Mixed Hearing Loss

    Dr. Scott E. Bevans, Dr. Brian S. Chen… in Encyclopedia of Otolaryngology, Head and N… (2013)

  12. No Access

    Living Reference Work Entry In depth

    Monteggia Fracture-Dislocations

    The Monteggia injury was initially described by Giovanni Monteggia as a proximal third ulnar fracture associated with a radial head dislocation. Since that time, the Monteggia fracture eponym has evolved to en...

    Dr. Lisa L. Lattanza, Dr. Sam Chen in The Pediatric Upper Extremity

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    Living Reference Work Entry In depth

    Embryology

    Developmental biology has greatly contributed to the understanding of upper limb development. Whereas early understanding of limb development centered on morphological change during organogenesis, current emph...

    Yen Hsun Chen, Aaron Daluiski in The Pediatric Upper Extremity

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    Reference Work Entry In depth

    Monteggia Fracture Dislocations

    The Monteggia injury was initially described by Giovanni Monteggia as a proximal third ulnar fracture associated with a radial head dislocation. Since that time, the Monteggia fracture eponym has evolved to en...

    Lisa L. Lattanza, Sam Chen in The Pediatric Upper Extremity (2015)

  15. No Access

    Reference Work Entry In depth

    Embryology

    Developmental biology has greatly contributed to the understanding of upper limb development. Whereas early understanding of limb development centered on morphological change during organogenesis, current emph...

    Yen Hsun Chen, Aaron Daluiski in The Pediatric Upper Extremity (2015)

  16. No Access

    Reference Work Entry In depth

    Congenital Cytomegalovirus Infection

    Congenital cytomegalovirus infection is the most common congenital infection in neonates in the USA, affecting approximately 0.5–1.5% of all live births and 30,000–40,000 newborns annually. Congenital infectio...

    Harold Chen in Atlas of Genetic Diagnosis and Counseling (2017)

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    Hypochondroplasia

    Hypochondroplasia (HCH) is a disproportionate short stature disorder resembling achondroplasia but with less severe phenotype.

    Harold Chen in Atlas of Genetic Diagnosis and Counseling (2017)

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    Reference Work Entry In depth

    Primary Microcephaly

    Primary microcephaly (MCPH) is a rare autosomal recessive neurodevelopmental disorder characterized by two principal features, microcephaly present at birth and nonprogressive mental retardation (Woods et al. ...

    Harold Chen in Atlas of Genetic Diagnosis and Counseling (2017)

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    Reference Work Entry In depth

    Hereditary Spastic Paraplegia

    The hereditary spastic paraplegia (HSP) are inherited disorders in which the primary neurological syndrome is bilateral, approximately symmetrical, lower-extremity spastic weakness, often accompanied by urinar...

    Harold Chen in Atlas of Genetic Diagnosis and Counseling (2017)

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    Reference Work Entry In depth

    R(18) Syndrome

    In 1962, Wang et al. (1962) reported the first observation of the ring chromosome 18. Ring chromosome 18 syndrome is a rare chromosome disorder resulting from loss (deletion) of genetic material from one or bo...

    Harold Chen in Atlas of Genetic Diagnosis and Counseling (2017)

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