A CASE OF PHENYLKETONURIA IN ETA RESULTING FROM MATING OF A HOMOZYGOUS FATHER AND A HETEROZYGOUS MOTHER

被引：0
|
作者：
FUJIKI, N
DREW, AL
NEMOTO, H
SHIMADA, T
MIYAKE, M
SUJAKU, C
机构：
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1961年 / 13卷 / 01期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：64 / &
相关论文
共 18 条
  • [1] A SEARCH FOR ASSORTATIVE MATING AND SEGREGATION ABNORMALITIES AMONG MOTHER-CHILD-FATHER TRIPLETS FROM PATERNITY CASES
    RASMUSON, M
    HED, H
    [J]. HEREDITAS, 1981, 94 (01) : 105 - 111
  • [2] Lethal thrombosis resulting from heterozygous tissue factor pathway inhibitor deficiency in homozygous factor V Leiden mice.
    Westrick, RJ
    Eitzman, DT
    Cui, JS
    Broze, GJ
    Ginsburg, D
    [J]. BLOOD, 1999, 94 (10) : 373A - 373A
  • [3] A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutation
    Yis, Uluc
    Uyanik, Gokhan
    Kurul, Semra
    Dirik, Eray
    Ozer, Erdener
    Gross, Claudia
    Hehr, Ute
    [J]. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2007, 11 (01) : 46 - 49
  • [4] NEONATAL ALLO-IMMUNE THROMBOCYTOPENIA DUE TO FETOMATERNAL HPA-1 INCOMPATIBILITY OF A HOMOZYGOUS HPA-1A MOTHER AND A HOMOZYGOUS HPA-1B FATHER - A CASE-REPORT
    MOSER, R
    FAE, I
    NEUMEISTER, A
    POBER, M
    MUTZ, I
    PANZER, S
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1994, 153 (02) : 95 - 97
  • [5] CFTR mutation analysis of a Caucasian father with congenital bilateral absence of vas deferens, a Taiwanese mother, and twins resulting from ICSI procedure
    Chiang, Han-Sun
    Wu, Chien-Chih
    Wu, Yi-No
    Lu, Jyh-Feng
    Lin, Gin-Hong
    Hwang, Jiann-Loung
    [J]. JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2008, 107 (09) : 736 - 740
  • [6] Educational Achievement of Children From Single-Mother and Single-Father Families: The Case of Japan
    Nonoyama-Tarumi, Yuko
    [J]. JOURNAL OF MARRIAGE AND FAMILY, 2017, 79 (04) : 915 - 931
  • [7] Genetic and Clinical Characteristics of Patients With Homozygous and Compound Heterozygous Familial Hypercholesterolemia From Three Different Populations: Case Series
    Marusic, Tatiana
    Sustar, Ursa
    Sadiq, Fouzia
    Kotori, Vjosa
    Mlinaric, Matej
    Kovac, Jernej
    Shafi, Saeed
    Khan, Iqbal
    Cevc, Matija
    Podkrajsek, Katarina Trebusak
    Battelino, Tadej
    Groselj, Urh
    [J]. FRONTIERS IN GENETICS, 2020, 11
  • [8] Different recurrence patterns after phototherapeutic keratectomy in the corneal dystrophy resulting from homozygous and heterozygous R124H BIG-H3 mutation
    Inoue, T
    Watanabe, H
    Yamamoto, S
    Inoue, Y
    Okada, M
    Hori, Y
    Maeda, N
    Inoue, Y
    Hayashi, K
    Shimomura, Y
    Tano, Y
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 2001, 132 (02) : 255 - 257
  • [9] A Case Series: A Mother and Daughter with a Critically Low Hemoglobin Level Resulting from Severe Anemia Secondary to Malaria
    Gutata, Dano
    [J]. INTERNATIONAL MEDICAL CASE REPORTS JOURNAL, 2024, 17 : 149 - 155
  • [10] Sodium taurocholate cotransporter polypeptide deficiency from two pairs of twins with homozygous and heterozygous of p.Ser267Phe variant, respectively: Case report
    Wang, Meifen
    Chen, Tao
    Li, Meirui
    Chen, Rui
    Peng, Junchao
    Li, Jiwei
    [J]. CLINICS AND RESEARCH IN HEPATOLOGY AND GASTROENTEROLOGY, 2024, 48 (03)
12