Autosomal dominant hypoparathyroidism associated with short stature and premature osteoarthritis.

被引：0
|
作者：
Stock, JL
Brown, RS
机构：
[1] MED CTR CENT MASSACHUSETTS,DIV ENDOCRINOL,WORCESTER,MA 01605
[2] UNIV MASSACHUSETTS,SCH MED,DEPT MED,WORCESTER,MA 01605
[3] UNIV MASSACHUSETTS,SCH MED,DEPT PEDIAT,WORCESTER,MA 01605
来源：
JOURNAL OF BONE AND MINERAL RESEARCH | 1996年 / 11卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：S500 / S500
页数：1
相关论文
共 50 条
  • [1] Autosomal dominant hypoparathyroidism associated with short stature and premature osteoarthritis
    Stock, JL
    Brown, RS
    Baron, J
    Coderre, JA
    Mancilla, E
    De Luca, F
    Ray, K
    Mericq, MV
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (09): : 3036 - 3040
  • [2] CORNEAL CHANGES, HYPERKERATOSIS, SHORT STATURE, BRACHYDACTYLY, AND PREMATURE BIRTH - A NEW AUTOSOMAL DOMINANT SYNDROME
    STERN, JK
    LUBINSKY, MS
    DURRIE, DS
    LUCKASEN, JR
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 18 (01): : 67 - 77
  • [3] AUTOSOMAL DOMINANT PARTIAL LIPODYSTROPHY ASSOCIATED WITH RIEGER ANOMALY, SHORT STATURE, AND INSULINOPENIC DIABETES
    AARSKOG, D
    OSE, L
    PANDE, H
    EIDE, N
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 15 (01): : 29 - 38
  • [4] Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension
    Toka, HR
    Bähring, S
    Chitayat, D
    Melby, JC
    Whitehead, R
    Jeschke, E
    Wienker, TF
    Toka, O
    Schuster, H
    Luft, FC
    ANNALS OF INTERNAL MEDICINE, 1998, 129 (03) : 204 - 208
  • [5] New autosomal dominant rhizo-mesomelic short stature syndrome.
    Azouz, EM
    Teebi, AS
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A91 - A91
  • [6] Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations
    Gkourogianni, Alexandra
    Andrew, Melissa
    Tyzinski, Leah
    Crocker, Melissa
    Douglas, Jessica
    Dunbar, Nancy
    Fairchild, Jan
    Funari, Mariana F. A.
    Heath, Karen E.
    Jorge, Alexander A. L.
    Kurtzman, Tracey
    LaFranchi, Stephen
    Lalani, Seema
    Lebl, Jan
    Lin, Yuezhen
    Los, Evan
    Newbern, Dorothee
    Nowak, Catherine
    Olson, Micah
    Popovic, Jadranka
    Pruhova, Stepanka
    Elblova, Lenka
    Quintos, Jose Bernardo
    Segerlund, Emma
    Sentchordi, Lucia
    Shinawi, Marwan
    Stattin, Eva-Lena
    Swartz, Jonathan
    Gonzalez del Angel, Ariadna
    Cuellar, Sinhue Diaz
    Hosono, Hidekazu
    Sanchez-Lara, Pedro A.
    Hwa, Vivian
    Baron, Jeffrey
    Nilsson, Ola
    Dauber, Andrew
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2017, 102 (02): : 460 - 469
  • [7] Identification of a Col2A1 mutation in a Micronesian family with autosomal dominant precocious osteoarthritis.
    Carlson, KM
    Reinker, K
    Person, D
    Abe, LM
    Perry, AK
    Yamaga, KM
    Marchuk, DA
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 212 - 212
  • [8] PRIMARY FAMILIAL HYPOPARATHYROIDISM WITH AN AUTOSOMAL DOMINANT MODE OF INHERITANCE
    DECAMPO, C
    PISCOPELLO, L
    NOACCO, C
    DACOL, P
    ENGLARO, GC
    BENEDETTI, A
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1988, 11 (02) : 91 - 96
  • [9] Autosomal Dominant Hypocalcemia (Hypoparathyroidism) Types 1 and 2
    Roszko, Kelly L.
    Bi, Ruiye D.
    Mannstadt, Michael
    FRONTIERS IN PHYSIOLOGY, 2016, 7
  • [10] DISTAL APHALANGIA, SYNDACTYLY, AND EXTRA METATARSAL, ASSOCIATED WITH SHORT STATURE, MICROCEPHALY, AND BORDERLINE INTELLIGENCE - A NEW AUTOSOMAL-DOMINANT DISORDER
    MARTINEZFRIAS, ML
    MARTIN, M
    PARDO, M
    DELASHERAS, FF
    FRIAS, JL
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 55 (02): : 213 - 216
12345