"X linked inhibitor" trang 1 - tải miễn phí từ tailieunhanh
Kiểu gen và kiểu hình của bệnh nhân X-linked adrenoleukodystrophy (X-ALD)

Kiểu gen và kiểu hình của bệnh nhân X-linked adrenoleukodystrophy (X-ALD)
5    65    1
Prenatal findings in a fetus with X-linked recessive type of chondrodysplasia punctata (CDPX1): A case report with novel mutation

Prenatal findings in a fetus with X-linked recessive type of chondrodysplasia punctata (CDPX1): A case report with novel mutation
6    80    0
Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: Report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein

Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: Report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein
6    43    0
A novel Bruton’s tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia

A novel Bruton’s tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia
5    91    0
Clinical and mutational features of Vietnamese children with X-linked agammaglobulinemia

Clinical and mutational features of Vietnamese children with X-linked agammaglobulinemia
5    49    0
Atypical X-linked agammaglobulinaemia caused by a novel BTK mutation in a selective immunoglobulin M deficiency patient

Atypical X-linked agammaglobulinaemia caused by a novel BTK mutation in a selective immunoglobulin M deficiency patient
6    75    0
Dosage sensitivity of X-linked genes in human embryonic single cells

Dosage sensitivity of X-linked genes in human embryonic single cells
9    38    1
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: A case report of twin brothers

A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: A case report of twin brothers
7    9    1
Extremely low nucleotide diversity in the X-linked region of papaya caused by a strong selective sweep

Extremely low nucleotide diversity in the X-linked region of papaya caused by a strong selective sweep
11    57    3
Allele-specific analysis of cell fusionmediated pluripotent reprograming reveals distinct and predictive susceptibilities of human X-linked genes to reactivation

Allele-specific analysis of cell fusionmediated pluripotent reprograming reveals distinct and predictive susceptibilities of human X-linked genes to reactivation
17    38    3
Báo cáo y học:

Báo cáo y học: "Dosage compensation on the active X chromosome minimizes transcriptional noise of X-linked genes in mammals"
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Fruitful analysis of sex chromosomes reveals X-treme genetic diversity

Fruitful analysis of sex chromosomes reveals X-treme genetic diversity
3    20    3
Báo cáo y học:

Báo cáo y học: "X-linked agammaglobulinemia diagnosed late in life: case report and review of the literature."
7    38    0
Một bệnh hiếm X-linked recessive hypoparathyroidism

Một bệnh hiếm X-linked recessive hypoparathyroidism
5    52    0
Báo cáo vật lý:

Báo cáo vật lý: "ATTENUATION STUDIES ON DRY AND HYDRATED CROSS-LINKED HYDROPHILIC COPOLYMER MATERIALS AT 8.02 TO 28.43 keV USING X-RAY FLUORESCENT SOURCES"
10    49    0
Báo cáo y học:

Báo cáo y học: "Recurrent pneumonia with mild hypogammaglobulinemia diagnosed as X-linked agammaglobulinemia in adults"
5    44    0
Báo cáo y học:

Báo cáo y học: " A three-year-old boy with X-linked adrenoleukodystrophy and congenital pulmonary adenomatoid malformation: a case report"
5    52    0
Báo cáo khoa học: Alpha-fetoprotein antagonizes X-linked inhibitor of apoptosis protein anticaspase activity and disrupts XIAP–caspase interaction

Báo cáo khoa học: Alpha-fetoprotein antagonizes X-linked inhibitor of apoptosis protein anticaspase activity and disrupts XIAP–caspase interaction
13    40    0
Ebook USMLE road map - Genetics: Part 1

Ebook USMLE road map - Genetics: Part 1
80    124    1
Clinical profile of comorbidity of rare diseases in a Tunisian patient: A case report associating incontinentia pigmenti and Noonan syndrome

Clinical profile of comorbidity of rare diseases in a Tunisian patient: A case report associating incontinentia pigmenti and Noonan syndrome
7    55    0