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27 April 2024

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Results 1 to 20 of 123 for query "M. Brothers". (0.00 sec.)

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Brother
Huntley, J.S.;

Wigner's Sisters
Y. S. Kim;
9 Mar 1997

Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus
W Rosenthal; A Seibold; A Antaramian; M Lonergan; M F Arthus; G N Hendy; M Birnbaumer; D G Bichet;
17 Sep 1992 / Nature, 359 (6392), 233-5

Purine overproduction in man associated with increased phosphoribosylpyrophosphate synthetase activity
M A Becker; L J Meyer; A W Wood; J E Seegmiller;
16 Mar 1973 / Science, 179 (78), 1123-6

Purine nucleoside phosphorylase deficiency: altered kinetic properties of a mutant enzyme
I H Fox; C M Andres; E W Gelf; D Biggar;
9 Sep 1977 / Science, 197 (4308), 1084-6

A linkage between DNA markers on the X chromosome and male sexual orientation
D H Hamer; S Hu; V L Magnuson; N Hu; A M Pattatucci;
16 Jul 1993 / Science, 261 (5119), 321-7

The chemistry of John Dalton's color blindness
D M Hunt; K S Dulai; J K Bowmaker; J D Mollon;
17 Feb 1995 / Science, 267 (5200), 984-8

Waldenstrom's macroglobulinaemia observed in two brothers
R MASSARI; J M FINE; R METAIS;
13 Oct 1962 / Nature, 196 (), 176-8

Inherited deletion of immunoglobulin heavy chain constant region genes in normal human individuals
M P Lefranc; G Lefranc; T H Rabbitts;
23 Dec 1982 / Nature, 300 (5894), 760-2

10.

Preferential deletion of exons in Duchenne and Becker muscular dystrophies
S M Forrest; G S Cross; A Speer; D Gardner-Medwin; J Burn; K E Davies;
15 Oct 1987 / Nature, 329 (6140), 638-40

11.

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
C Larsson; B Skogseid; K Oberg; Y Nakamura; M Nordenskjöld;
3 Mar 1988 / Nature, 332 (6159), 85-7

12.

Genetic evidence equating SRY and the testis-determining factor
P Berta; J R Hawkins; A H Sinclair; A Taylor; B L Griffiths; P N Goodfellow; M Fellous;
29 Nov 1990 / Nature, 348 (6300), 448-50

13.

Decreased platelet inhibition by nitric oxide in two brothers with a history of arterial thrombosis.
Freedman, J E; Loscalzo, J; Benoit, S E; Valeri, C R; Barnard, M R; Michelson, A D;

14.

Premature termination codons on both alleles of the type VII collagen gene (COL7A1) in three brothers with recessive dystrophic epidermolysis bullosa.
Christiano, A M; Suga, Y; Greenspan, D S; Ogawa, H; Uitto, J;

15.

Search for the pathogenesis of the differing phenotype in two compound heterozygote Hungarian brothers with the same genotypic triosephosphate isomeraseâ€‰deficiency
HollÃ¡n, Susan; MagÃ³csi, MÃ¡ria; Fodor, Elfrieda; HorÃ¡nyi, Margit; HarsÃ¡nyi, Veronika; Farkas, Tibor;

16.

Blood-Brothers; an Ethno-sociological Study of the Institutions of Blood-Brotherhood, with Special Reference to Africa
Setzler, F. M.;

17.

The Cuspy LINER Nucleus of the S0/a Galaxy NGC 2681
Michele Cappellari; Francesco Bertola; David Burstein; Lucio M. Buson; Laura Greggio; Alvio Renzini;
20 Dec 2000

18.

Diffusion controlled initial recombination
T. Christen; M. Buttiker;
31 Oct 1997 / Phys. Rev. E58, 1533 (1998)

19.

The Square-Lattice Heisenberg Antiferromagnet at Very Large Correlation Lengths
B. B. Beard; R. J. Birgeneau; M. Greven; U.-J. Wiese;
9 Sep 1997

20.

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
J Mosser; A M Douar; C O Sarde; P Kioschis; R Feil; H Moser; A M Poustka; J L Mandel; P Aubourg;
25 Feb 1993 / Nature, 361 (6414), 726-30

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