A Gene for Autosomal Dominant Congenital Nystagmus Localizes to 6p12

By Kerrison J.B.   Arnould V.J.   Barmada M.M.   Koenekoop R.K.   Schmeckpeper B.J.   Maumenee I.H.  

Genomics, Vol. 33, Iss. 3, 1996-05 ,pp. : 523-526

Academic Press

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Chromosomal Mapping of Two Members of the Human Dynein Gene Family to Chromosome Regions 7p15 and 11q13 near the Deafness Loci DFNA 5 and DFNA 11

By Kastury K.   Taylor W.E.   Gutierrez M.   Ramirez L.   Coucke P.J.   van Hauwe P.   van Camp G.   Bhasin S.  

Genomics, Vol. 44, Iss. 3, 1997-09 ,pp. : 362-364

Academic Press

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Physical and Radiation Hybrid Mapping of Canine Chromosome 12, in a Region Corresponding to Human Chromosome 6p12-q12

By Li R.   Faraco J.H.   Lin L.   Lin X.   Hinton L.   Rogers W.   Lowe J.K.   Ostrander E.A.   Mignot E.  

Genomics, Vol. 73, Iss. 3, 2001-05 ,pp. : 299-315

Elsevier

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Assignment of Human Protein Phosphatase 2A Regulatory Subunit Genes B56alpha, B56beta, B56gamma, B56delta, and B56epsi (PPP2R5A-PPP2R5E), Highly Expressed in Muscle and Brain, to Chromosome Regions 1q41, 11q12, 3p21, 6p21.1, and 7p11.2 -< p12

By McCright B.   Brothman A.R.   Virshup D.M.  

Genomics, Vol. 36, Iss. 1, 1996-08 ,pp. : 168-170

Academic Press

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Identification of a New Locus for Autosomal Recessive Charcot-Marie-Tooth Disease with Focally Folded Myelin on Chromosome 11p15

By Othmane K.B.   Johnson E.   Menold M.   Graham F.L.   Hamida M.B.   Hasegawa O.   Rogala A.D.   Ohnishi A.   Pericak-Vance M.   Hentati F.   Vance J.M.  

Genomics, Vol. 62, Iss. 3, 1999-12 ,pp. : 344-349

Elsevier

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