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Sex Chromosome Disorders
Clinical conditions caused by an abnormal sex chromosome constitution (SEX CHROMOSOME ABERRATIONS), in which there is extra or missing sex chromosome material (either a whole chromosome or a chromosome segment).
推出的年份: 2002
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C16.131.260.830, C16.320.180.830
MeSH 单一 ID:
D025064
进入的组:
Disorders, Sex Chromosome Abnormality
Sex Chromosome Abnormality Disorders
Disorders, Sex Chromosome
Chromosome Disorder, Sex
Chromosome Disorders, Sex
Sex Chromosome Disorder
早前的内容:
Sex Chromosome Abnormalities (1971-2001)
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Chromosome Disorders [C16.131.260]
22q11 Deletion Syndrome [C16.131.260.019]
add_circle
Angelman Syndrome [C16.131.260.040]
Beckwith-Wiedemann Syndrome [C16.131.260.080]
Branchio-Oto-Renal Syndrome [C16.131.260.090]
Cri-du-Chat Syndrome [C16.131.260.190]
De Lange Syndrome [C16.131.260.210]
Down Syndrome [C16.131.260.260]
Holoprosencephaly [C16.131.260.380]
Jacobsen Distal 11q Deletion Syndrome [C16.131.260.440]
Prader-Willi Syndrome [C16.131.260.700]
Rubinstein-Taybi Syndrome [C16.131.260.790]
Sex Chromosome Disorders [C16.131.260.830]
Fragile X Syndrome [C16.131.260.830.300]
Orofaciodigital Syndromes [C16.131.260.830.670]
Sex Chromosome Disorders of Sex Development [C16.131.260.830.835]
add_circle
Silver-Russell Syndrome [C16.131.260.870]
Smith-Magenis Syndrome [C16.131.260.887]
Sotos Syndrome [C16.131.260.905]
Trisomy 13 Syndrome [C16.131.260.923]
Trisomy 18 Syndrome [C16.131.260.932]
WAGR Syndrome []
add_circle
Williams Syndrome [C16.131.260.970]
Wolf-Hirschhorn Syndrome [C16.131.260.985]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Chromosome Disorders [C16.320.180]
22q11 Deletion Syndrome [C16.320.180.019]
add_circle
Angelman Syndrome [C16.320.180.040]
Beckwith-Wiedemann Syndrome [C16.320.180.080]
Branchio-Oto-Renal Syndrome [C16.320.180.090]
Cri-du-Chat Syndrome [C16.320.180.190]
De Lange Syndrome [C16.320.180.210]
Down Syndrome [C16.320.180.260]
Holoprosencephaly [C16.320.180.380]
Jacobsen Distal 11q Deletion Syndrome [C16.320.180.440]
Prader-Willi Syndrome [C16.320.180.700]
Rubinstein-Taybi Syndrome [C16.320.180.790]
Sex Chromosome Disorders [C16.320.180.830]
Fragile X Syndrome [C16.320.180.830.300]
Orofaciodigital Syndromes [C16.320.180.830.670]
Sex Chromosome Disorders of Sex Development [C16.320.180.830.835]
add_circle
Silver-Russell Syndrome [C16.320.180.870]
Smith-Magenis Syndrome [C16.320.180.887]
Sotos Syndrome [C16.320.180.905]
Trisomy 13 Syndrome [C16.320.180.923]
Trisomy 18 Syndrome [C16.320.180.932]
WAGR Syndrome []
add_circle
Williams Syndrome [C16.320.180.970]
Wolf-Hirschhorn Syndrome [C16.320.180.985]
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