PMID- 10343123
OWN - NLM
STAT- MEDLINE
DCOM- 19990625
LR  - 20171101
IS  - 0301-0171 (Print)
IS  - 0301-0171 (Linking)
VI  - 84
IP  - 1-2
DP  - 1999
TI  - HOX11L1, a gene involved in peripheral nervous system development, maps to human 
      chromosome 2p13.1-->p12 and mouse chromosome 6C3-D1.
PG  - 115-7
AB  - HOX11L1 is a homeobox gene involved in peripheral nervous system development as
      confirmed by knockout mice exhibiting megacolon with enteric ganglia, a phenotype
      associated in human with Intestinal Neuronal Dysplasia (IND). Using FISH and
      radiation hybrids we have localized HOX11L1 to human chromosome 2p13.1-->p12, in 
      a 14-cR interval between WI-5987 (D2S2088) and GCT1B4 (D2S2497), and confirmed
      the synteny between mouse 6C3-D1 and human 2p13.1-->p12 chromosomes by mapping an
      EST cDNA clone corresponding to mouse HOX11L1 (Tlx2).
FAU - Puliti, A
AU  - Puliti A
AD  - Laboratorio di Genetica Molecolare, Istituto Giannina Gaslini, Genova-Quarto,
      Italy.
FAU - Cinti, R
AU  - Cinti R
FAU - Betsos, N
AU  - Betsos N
FAU - Romeo, G
AU  - Romeo G
FAU - Ceccherini, I
AU  - Ceccherini I
LA  - eng
GR  - E.0791/Telethon/Italy
PT  - Comparative Study
PT  - Journal Article
PT  - Research Support, Non-U.S. Gov't
PL  - Switzerland
TA  - Cytogenet Cell Genet
JT  - Cytogenetics and cell genetics
JID - 0367735
RN  - 0 (DNA Primers)
SB  - IM
MH  - Animals
MH  - Base Sequence
MH  - Chromosome Banding
MH  - Chromosome Mapping
MH  - Chromosomes, Human, Pair 2/*genetics
MH  - DNA Primers/genetics
MH  - *Genes, Homeobox
MH  - Humans
MH  - Hybrid Cells
MH  - In Situ Hybridization, Fluorescence
MH  - Intestines/innervation/pathology
MH  - Mice/*genetics
MH  - Mice, Knockout
MH  - Phenotype
MH  - Species Specificity
EDAT- 1999/05/27 06:00
MHDA- 2000/08/16 11:00
CRDT- 1999/05/27 06:00
PHST- 1999/05/27 06:00 [pubmed]
PHST- 2000/08/16 11:00 [medline]
PHST- 1999/05/27 06:00 [entrez]
AID - 15234 [pii]
AID - 10.1159/000015234 [doi]
PST - ppublish
SO  - Cytogenet Cell Genet. 1999;84(1-2):115-7. doi: 10.1159/000015234.