PMID- 10337628
OWN - NLM
STAT- MEDLINE
DCOM- 19990708
LR  - 20190905
IS  - 0938-8990 (Print)
IS  - 0938-8990 (Linking)
VI  - 10
IP  - 5
DP  - 1999 May
TI  - Mapping of the otogelin gene (OTGN) to mouse chromosome 7 and human chromosome
      11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18.
PG  - 520-2
FAU - Cohen-Salmon, M
AU  - Cohen-Salmon M
AD  - Unite de Genetique des Deficits Sensoriels, CNRS URA 1968, Institut Pasteur,
      Paris, France.
FAU - Mattei, M G
AU  - Mattei MG
FAU - Petit, C
AU  - Petit C
LA  - eng
PT  - Journal Article
PL  - United States
TA  - Mamm Genome
JT  - Mammalian genome : official journal of the International Mammalian Genome Society
JID - 9100916
RN  - 0 (Membrane Glycoproteins)
RN  - 0 (OTOG protein, human)
RN  - 0 (Otog protein, mouse)
SB  - IM
MH  - Animals
MH  - Blotting, Southern
MH  - *Chromosome Mapping
MH  - *Chromosomes, Human, Pair 11
MH  - Deafness/*genetics
MH  - *Genes, Recessive
MH  - Humans
MH  - Hybrid Cells
MH  - In Situ Hybridization, Fluorescence
MH  - Membrane Glycoproteins/*genetics
MH  - Mice
EDAT- 1999/05/25 00:00
MHDA- 1999/05/25 00:01
CRDT- 1999/05/25 00:00
PHST- 1999/05/25 00:00 [pubmed]
PHST- 1999/05/25 00:01 [medline]
PHST- 1999/05/25 00:00 [entrez]
AID - 10.1007/s003359901033 [doi]
PST - ppublish
SO  - Mamm Genome. 1999 May;10(5):520-2. doi: 10.1007/s003359901033.