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PT3699-3E (PR27547) Hu Plas 12K page 142
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author: emmachleder
updated: 22/08/2002
matching:
split hand foot malform ectrodactyli type 3
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http://www.clontech.com/clontech/atlas/genelists/7931-1_HuPlastic12K.txt
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article ID:
updated: 22/08/2002
matching:
split hand malform ectrodactyli type 3
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SHFM3P1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
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author: Abnova
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FBXW4 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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12710 Flint Place
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author: Kirsten
updated: 07/10/2005
matching:
split hand foot malform
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Genetic Disease Markers
- - <%-- ************************************************************ HTML Content Started Here ************************************************************ --%> Category :- Genetic Disease Markers Search Result Product Catalog# Unit Price Add To Cart Adenosine deaminase (ADA) polyclonal antibody PAB-10464 $150.00 ADP-ribosyltransferase (ADPRT) polyclonal antibody PAB-10561 $150.00...
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NTD Bibliographical References from 1994 - The Jackson Laboratory
Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations.
Split hand/split foot, syndactyly, urinary tract obstruction, radial, diaphragmatic, and neural tube defects: Czeizel-Losonci syndrome?.
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DLX5 Recombinant Protein (P01)-Abnova Corporation
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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Lab Vision Corporation
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Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly.
DLX5 is a candidate gene for split-hand/split-foot malformation (SHFM1).
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DLX5 Recombinant Protein
CXCR4 Antibody, CXCR4 Antibodies Committed to bringing you the highest quality research products - - - - - - - - - Catalog No.: XW-rP3064 DLX5 (Human), Recombinant Protein , E.
DLX5 is a candidate gene for split-hand/split-foot malformation (SHFM1).
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