Terminal 22q deletion associated with a partial deficiency of arylsulphatase A.

Author:

Narahara K,Takahashi Y,Murakami M,Tsuji K,Yokoyama Y,Murakami R,Ninomiya S,Seino Y

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome;Watt, J.L.; Olson, I.A.; Johnston, A.W.; Ross, H.S.; Couzin, D.A.; Stephen, G.S.;7 Med Genet,1985

2. Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q);Herman, G.E.; Greenberg, F.; Ledbetter, D.H.;Am J7 Med Genet,1988

3. New method for determining ferrihemoglobn reductase (NADH methemoglobin reductase) in erythrocytes;Hegesh, E.; Calmanovici, N.; Avron, M.;Jf Lab Clin Med,1968

4. Genetic metabolic disease;Galjaard, H.,1982

5. Determination of the breakpoints and the parental origin of a ring 22 chromosome: an analysis by high-resolution banding techniques, quinacrine and silver stainings;Naritomi, K.; Hirayama, K.;Jpn J Hum Genet,1988

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