Reorganization plan no. 1 of 1950 : providing for reorganizations in the Department of the Treasury : report, together with the minority views (to accompany S. Res. 246)

Also in Congressional serial volume 11368.

Violations of free speech and rights of labor : digest of report of the Committee on Education and Labor pursuant to S. Res. 246 (74th Congress)

At head of title: 76th Congress, 1st session. Senate committee print.

Wild-life conservation. Report [pursuant to S. Res. 246]

Mode of access: Internet.

How can the health care of United States citizens best be improved? : a collection of excerpts and bibliography relating to the high school debate topic, 1977-1978, pursuant to Public Law 88-246 /

Mode of access: Internet.

Operator's manual : drilling system, well, rotary, truck mounted, air transportable, 600 feet capacity : model LP-12, NSN 3820-01-246-4276.

Includes index.

Organizational and direct support maintenance repair parts and special tools list : kitchen, field, trailer mounted, MKT-75 (NSN 7360-00-138-7782) ... MKT-85S (NSN 7360-01-246-4646).

Includes indexes.

Organizational maintenance manual : telegraph terminal TH-5/TG (NSN 5805-00-315-2858), TH-5A/TG (NSN 5805-00-246-8734).

Includes index.

Direct support and general support maintenance repair parts and special tools lists ... : terminals, telegraph TH-5/TG (FSN 5805-246-8734) and TH-5A/TG (FSN 5805-020-5720).

"31 July 1973."

Direct support and general support maintenance repair parts and special tools list (including depot maintenance repair parts and special tools) for receiver-transmitter radio RT-246/VRC, RT-246A/VRC, (NSN 5820-00-892-0623).

"31 January 1983."

Direct support and general support maintenance manual : radio sets AN/VRC-12 (NSN 5820-00-223-7412), AN/VRC-43 (NSN 5820-00-223-7415), AN/VRC-44 (NSN 5820-00-223-7417 ... receiver-transmitters, radio RT-246/VRC ....

"16 April 1984"--Vol. 1.

Operator's manual : terminal, radio-telephone, mobile subscriber AN/VRC-97 (NSN 5820-01-246-6818) and installation kit, electronic equipment MK-2564/VRC-97 and MK-2565/VRC-97 (NSN 5820-01-246-6873).

"1 March 1989."

Resolución 246 del 02 de noviembre de 2007: ¿Cuáles son los criterios que tiene en cuenta la Cámara de Comercio para llevar a cabo el control de legalidad de la cesión de cuotas?

Servicios registrales

Resolución 246 del 05 de diciembre de 2008: Por medio de la cual se ordena adicionar un registro

Doctrina

Nodulação da cultivar de soja BRS 246 RR tratada com diferentes inoculantes comerciais em terras baixas.

2015

Pyrimidine-5'-nucleotidase Campinas, A New Mutation (p.r56g) In The Nt5c3 Gene Associated With Pyrimidine-5'-nucleotidase Type I Deficiency And Influence Of Gilbert's Syndrome On Clinical Expression.

Pyrimidine-5'-nucleotidase type I (P5'NI) deficiency is an autosomal recessive condition that causes nonspherocytic hemolytic anemia, characterized by marked basophilic stippling and pyrimidine nucleotide accumulation in erythrocytes. We herein present two African descendant patients, father and daughter, with P5'N deficiency, both born from first cousins. Investigation of the promoter polymorphism of the uridine diphospho glucuronosyl transferase 1A (UGT1A) gene revealed that the father was homozygous for the allele (TA7) and the daughter heterozygous (TA6/TA7). P5'NI gene (NT5C3) gene sequencing revealed a further change in homozygosity at amino acid position 56 (p.R56G), located in a highly conserved region. Both patients developed gallstones; however the father, who had undergone surgery for the removal of stones, had extremely severe intrahepatic cholestasis and, liver biopsy revealed fibrosis and siderosis grade III, leading us to believe that the homozygosity of the UGT1A polymorphism was responsible for the more severe clinical features in the father. Moreover, our results show how the clinical expression of hemolytic anemia is influenced by epistatic factors and we describe a new mutation in the P5'N gene associated with enzyme deficiency, iron overload, and severe gallstone formation. To our knowledge, this is the first description of P5'N deficiency in South Americans.